Analyses of MMP20 Missense Mutations in Two Families with Hypomaturation Amelogenesis Imperfecta

about

The Presence of MMP-20 Reinforces Biomimetic Enamel Regrowth.

P2860

Q38636745-CCEEC092-6E9E-483F-A302-DEDA1E21B52C

P2860

Analyses of MMP20 Missense Mutations in Two Families with Hypomaturation Amelogenesis Imperfecta

Item

http://www.wikidata.org/entity/Q33580860

description

2017 nî lūn-bûn

@nan

2017 թուականի Ապրիլին հրատարակուած գիտական յօդուած

@hyw

2017 թվականի ապրիլին հրատարակված գիտական հոդված

@hy

2017年の論文

@ja

2017年論文

@yue

2017年論文

@zh-hant

2017年論文

@zh-hk

2017年論文

@zh-mo

2017年論文

@zh-tw

2017年论文

@wuu

name

Analyses of MMP20 Missense Mut ...... ration Amelogenesis Imperfecta

@ast

Analyses of MMP20 Missense Mut ...... ration Amelogenesis Imperfecta

@en

Analyses of MMP20 Missense Mut ...... ation Amelogenesis Imperfecta.

@nl

type

Item

label

Analyses of MMP20 Missense Mut ...... ration Amelogenesis Imperfecta

@ast

Analyses of MMP20 Missense Mut ...... ration Amelogenesis Imperfecta

@en

Analyses of MMP20 Missense Mut ...... ation Amelogenesis Imperfecta.

@nl

prefLabel

Analyses of MMP20 Missense Mut ...... ration Amelogenesis Imperfecta

@ast

Analyses of MMP20 Missense Mut ...... ration Amelogenesis Imperfecta

@en

Analyses of MMP20 Missense Mut ...... ation Amelogenesis Imperfecta.

@nl

P1476

Analyses of MMP20 Missense Mut ...... ration Amelogenesis Imperfecta

@en

P2093

Figen Seymen

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

James P Simmer

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

Jan C-C Hu

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

Jenny Kang

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

Jung-Wook Kim

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

Koray Gencay

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

Mine Koruyucu

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

Teo Jeon Shin

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

Youn Jung Kim

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

Zang Hee Lee

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

P2860

Mutation in kallikrein 4 causes autosomal recessive hypomaturation amelogenesis imperfecta

Identification and structural and functional characterization of human enamelysin (MMP-20)

A deletion in the amelogenin gene (AMG) causes X-linked amelogenesis imperfecta (AIH1)

ITGB6 loss-of-function mutations cause autosomal recessive amelogenesis imperfecta

MMP20 hemopexin domain mutation in amelogenesis imperfecta

FAM83H mutations in families with autosomal-dominant hypocalcified amelogenesis imperfecta

Mutations in the beta propeller WDR72 cause autosomal-recessive hypomaturation amelogenesis imperfecta

MMP-20 mutation in autosomal recessive pigmented hypomaturation amelogenesis imperfecta

Compound heterozygosity for a dominant glycine substitution and a recessive internal duplication mutation in the type XVII collagen gene results in junctional epidermolysis bullosa and abnormal dentition

Identification of mutations in SLC24A4, encoding a potassium-dependent sodium/calcium exchanger, as a cause of amelogenesis imperfecta

P304

229

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

P31

scholarly article

P356

10.3389/FPHYS.2017.00229

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

P478

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

P50

Hong-Keun Hyun

P577

2017-04-20T00:00:00Z

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

P698

28473773

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

P921

hypomaturation amelogenesis imperfecta

P932

5397402

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

Analyses of MMP20 Missense Mutations in Two Families with Hypomaturation Amelogenesis Imperfecta

about

P2860

P2860

Analyses of MMP20 Missense Mutations in Two Families with Hypomaturation Amelogenesis Imperfecta

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P478

P50

P577

P698

P921

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P478

P50

P577

P698

P921

P932