Novel domain-specific POU3F4 mutations are associated with X-linked deafness: examples from different populations. - Wikidata - awgldk - TriplyDB

Novel domain-specific POU3F4 mutations are associated with X-linked deafness: examples from different populations.

Novel domain-specific POU3F4 mutations are associated with X-linked deafness: examples from different populations.

http://www.wikidata.org/entity/Q30412441

about

A POU3F4 Mutation Causes Nonsyndromic Hearing Loss in a Chinese X-linked Recessive Family.Medical genetics and genomic medicine in Nigeria.Clinical and molecular characterization of POU3F4 mutations in multiple DFNX2 Chinese families

P2860

Q30363026-6986C444-B9DC-49D5-BE13-1F9C6438C9E9 Q55437215-BF3E6C22-D2B5-4D09-8F63-837C20AD5502 Q58765599-179F1C74-2860-4009-B418-C1B20E9E3ADC

P2860

Novel domain-specific POU3F4 mutations are associated with X-linked deafness: examples from different populations.

http://www.wikidata.org/entity/Q30412441

description

2015 nî lūn-bûn

@nan

2015 թուականի Փետրուարին հրատարակուած գիտական յօդուած

@hyw

2015 թվականի փետրվարին հրատարակված գիտական հոդված

@hy

2015年の論文

@ja

2015年論文

@yue

2015年論文

@zh-hant

2015年論文

@zh-hk

2015年論文

@zh-mo

2015年論文

@zh-tw

2015年论文

@wuu

name

Novel domain-specific POU3F4 m ...... es from different populations.

@ast

Novel domain-specific POU3F4 m ...... es from different populations.

@en

type

label

Novel domain-specific POU3F4 m ...... es from different populations.

@ast

Novel domain-specific POU3F4 m ...... es from different populations.

@en

prefLabel

Novel domain-specific POU3F4 m ...... es from different populations.

@ast

Novel domain-specific POU3F4 m ...... es from different populations.

@en

P1433

Q30412441-F382A04F-CE19-484A-AB5E-E460E030E259

P1476

Q30412441-C2F08EE9-1B7E-4FBC-B9C4-0700402DB2AB

P2093

Q30412441-11594855-0A48-4BFF-A388-88786D42EA32

Q30412441-259167C0-5699-4238-8F33-14B27BC7A29F

Q30412441-2ABA87E0-7A6F-4C8B-B993-551DA1222D0B

Q30412441-2BB5E6FB-A082-45ED-BB19-DF2FEB071158

Q30412441-51DB7083-91A9-415B-8A90-1EDCF380D29D

Q30412441-69F72B2C-E667-4D58-87AB-9A22141CE26C

Q30412441-A10CC1B6-A24E-4877-BD2D-07DA637C27BF

Q30412441-BAB86C35-7DC2-417F-AE8D-BB9711F48660

Q30412441-BCE1BB70-8DD3-4E4A-8174-B2F0FF175D45

Q30412441-E5275883-1C37-49C8-8D25-2D61C7A09ED8

P2860

Q30412441-052629FF-A605-49C2-B670-6D493DE6E0C4

Q30412441-0DB5DCF3-F098-4618-A9D3-789BAEA298B7

Q30412441-11AD1FBC-D6B5-4034-A0CD-181E90A5C31D

Q30412441-141B4ADA-00CA-4D18-8F41-92E322B30C58

Q30412441-3D6F4D01-7EC3-481B-8BA9-CCA03C96140C

Q30412441-3DD7EE80-58AF-4F2A-A177-34FA0D0DB7A9

Q30412441-540953B2-7947-4F93-973D-8B12E307DFA3

Q30412441-55458010-FCEE-4996-8256-DF4C227004C8

Q30412441-6703DEE0-DBD6-4103-A50A-40B4567B6DA1

Q30412441-7A92366C-09F8-4804-A161-16644F51B6A2

P2888

Q30412441-47FF8A5B-4529-4FFE-ADBD-290616FEB0B9

P304

Q30412441-BC88884B-0DE7-4723-928C-C40E4A1B3C95

P31

Q30412441-ADFAEC9E-4BB2-4B2E-8B89-FDF44B48898B

P356

Q30412441-F5EA7B6A-1F6C-450F-BC22-548F64CA0E99

P478

Q30412441-6D5FBCC8-6377-4914-BA08-F0351485636C

P50

Q30412441-03F9A707-7A2F-478E-A491-67563E4F49CE

Q30412441-62EFB7C0-5859-44B0-A604-A4002FD45F69

Q30412441-69566E2B-6E30-4205-A3EF-E104E4908DB2

Q30412441-8DEB1664-CDFE-425B-BD8D-AEDFAA359F9C

P577

Q30412441-CC7FD299-490B-4DE1-A51A-3E477EE74EC4

P5875

Q30412441-9C9908AC-4A3E-4FB9-821A-7C29C695501F

P6179

Q30412441-872370FB-8A45-40EC-9B2A-E149D18495EE

P698

Q30412441-ED07233C-B1FD-4663-A6CC-36BE69C38C3C

P932

Q30412441-71124046-C32C-4332-82A2-DC6AA142FFB4

P356

S12881-015-0149-2

P1433

BMC Medical Genetics

P1476

Novel domain-specific POU3F4 m ...... es from different populations.

@en

P2093

Akeem Lasisi

http://www.w3.org/2001/XMLSchema#string

Armagan Incesulu

http://www.w3.org/2001/XMLSchema#string

Asli Subasioglu

http://www.w3.org/2001/XMLSchema#string

Ibis Menendez

http://www.w3.org/2001/XMLSchema#string

Kemal O Yariz

http://www.w3.org/2001/XMLSchema#string

Levent Sennaroglu

http://www.w3.org/2001/XMLSchema#string

Paola Montenegro

http://www.w3.org/2001/XMLSchema#string

Rodrigo Vinueza

http://www.w3.org/2001/XMLSchema#string

Suat Fitoz

http://www.w3.org/2001/XMLSchema#string

Susan Blanton

http://www.w3.org/2001/XMLSchema#string

P2860

Brain 4: a novel mammalian POU domain transcription factor exhibiting restricted brain-specific expression

RHS2, a POU domain-containing gene, and its expression in developing and adult rat

Loss-of-function mutations in the PRPS1 gene cause a type of nonsyndromic X-linked sensorineural deafness, DFN2

Association between X-linked mixed deafness and mutations in the POU domain gene POU3F4

Changes in the subcellular localization of the Brn4 gene product precede mesenchymal remodeling of the otic capsule

A new mutation in the POU3F4 gene in a Japanese family with X-linked mixed deafness (DFN3)

Further mutations in Brain 4 (POU3F4) clarify the phenotype in the X-linked deafness, DFN3

POU domain transcription factor brain 4 confers pancreatic alpha-cell-specific expression of the proglucagon gene through interaction with a novel proximal promoter G1 element

Cytoplasmic mislocalization of POU3F4 due to novel mutations leads to deafness in humans and mice.

Whole-exome sequencing efficiently detects rare mutations in autosomal recessive nonsyndromic hearing loss.

P2888

s12881-015-0149-2

P304

9

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1186/S12881-015-0149-2

http://www.w3.org/2001/XMLSchema#string

P478

16

http://www.w3.org/2001/XMLSchema#string

P50

Rosario Paredes

Germania Moreta

P577

2015-02-25T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P5875

275666261

http://www.w3.org/2001/XMLSchema#string

P6179

1046938945

http://www.w3.org/2001/XMLSchema#string

P698

25928534

http://www.w3.org/2001/XMLSchema#string

P932

4422282

http://www.w3.org/2001/XMLSchema#string