Central areolar choroidal dystrophy associated with dominantly inherited drusen. - Wikidata - wikimedia - TriplyDB

Central areolar choroidal dystrophy associated with dominantly inherited drusen.

Central areolar choroidal dystrophy associated with dominantly inherited drusen.

http://www.wikidata.org/entity/Q33956940

about

Central areolar choroidal dystrophy associated with inherited drusen in a multigeneration Tunisian family: exclusion of the PRPH2 gene and the 17p13 locus.Central areolar choroidal dystrophy with associated dominant drusen.A long history of dense deposit disease

P2860

Q39330616-4A9E74E0-6941-47CD-9B8D-8C1640DB012E Q55428824-06D94657-3A72-4FCD-9F6E-8FD5DD7D18B7 Q58739269-0A1FB0D9-7FE1-4139-B408-477D4851CA55

P2860

Central areolar choroidal dystrophy associated with dominantly inherited drusen.

http://www.wikidata.org/entity/Q33956940

description

2002 nî lūn-bûn

@nan

2002 թուականի Յունուարին հրատարակուած գիտական յօդուած

@hyw

2002 թվականի հունվարին հրատարակված գիտական հոդված

@hy

2002年の論文

@ja

2002年学术文章

@wuu

2002年学术文章

@zh-cn

2002年学术文章

@zh-hans

2002年学术文章

@zh-my

2002年学术文章

@zh-sg

2002年學術文章

@yue

name

Central areolar choroidal dystrophy associated with dominantly inherited drusen.

@ast

Central areolar choroidal dystrophy associated with dominantly inherited drusen.

@en

type

label

Central areolar choroidal dystrophy associated with dominantly inherited drusen.

@ast

Central areolar choroidal dystrophy associated with dominantly inherited drusen.

@en

prefLabel

Central areolar choroidal dystrophy associated with dominantly inherited drusen.

@ast

Central areolar choroidal dystrophy associated with dominantly inherited drusen.

@en

P1433

Q33956940-EC23320C-4A75-426B-92AD-D822613CB566

P1476

Q33956940-D8BDD4D4-320D-4947-8E3F-646D8C0D63F7

P2093

Q33956940-0009B876-0610-4A9F-8631-79BF67CC061C

Q33956940-0518DF8C-CDF0-4A23-9B0C-749B899B581C

Q33956940-82B4FFD5-EBBE-453D-93EB-BF6C8B093BC0

Q33956940-97DD8DD8-97C4-4B9D-9EA5-7F7C3E00DD6B

Q33956940-AADF0132-3DD4-4A40-8FD0-3FD2F123B9B6

Q33956940-EC4F4CB6-8735-4407-B158-5DC74830D21F

Q33956940-F186B9DD-84CC-4232-BD95-3D7E6B16A2BB

Q33956940-FFFC2BB2-B7F4-4C77-AAB8-6EE5D714A476

P2860

Q33956940-03D6AD2B-ABD6-496F-A069-7F932793DA8E

Q33956940-0D0F5ACD-A288-44B2-A52A-415FC1142E27

Q33956940-1B5D5044-0829-4B03-876B-CE858FB711A6

Q33956940-1C677A93-8861-47D6-A8ED-ECD4C9AFCE24

Q33956940-224EA671-2132-4B44-95F6-CCEE2979D009

Q33956940-366B0312-3C12-4890-9C15-42B3D0A19FC3

Q33956940-4F60B6D7-1E0C-4796-8D57-E7AD6573D5DF

Q33956940-73F22C67-D4E1-4AE3-95EE-C7A431FA3353

Q33956940-8F115D62-A554-4B9B-9406-F834558E14BA

Q33956940-910C9E35-D299-4987-AE32-2FEAD34CD7F4

P304

Q33956940-044C0804-5099-46E1-BCE6-B932FB0E82A9

P31

Q33956940-60C22D24-1338-4079-9C52-92A06135D04A

P356

Q33956940-428AB881-EDAE-486E-9E9F-B982852C247F

P407

Q33956940-B3A78E7C-103D-44F0-BB3D-BBFFEC59E43C

P433

Q33956940-8282AA05-410D-43AB-A6A9-2EFEB218F842

P478

Q33956940-7D4A9AC5-6215-4E52-BBDC-5D265383BDE6

P577

Q33956940-7415A7AF-E6A8-43DB-85FF-FA6D60A9E69A

P5875

Q33956940-F4EF4C68-9ED4-4FA8-9DAB-1D0B3AF142F4

P698

Q33956940-5E1CDA5D-D318-435D-9756-28BEB511EE54

P932

Q33956940-63CABA7C-8A57-49BF-A07F-B53629F35FEC

P356

P1433

British Journal of Ophthalmology

P1476

Central areolar choroidal dystrophy associated with dominantly inherited drusen.

@en

P2093

Alfred J L G Pinckers

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

August F Deutman

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

August J M van Hogerwou

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

B Jeroen Klevering

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

Carel B Hoyng

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

Dorien J R van De Pol

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

Frans P M Cremers

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

Marc van Driel

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

P2860

A single EFEMP1 mutation associated with both Malattia Leventinese and Doyne honeycomb retinal dystrophy

Mutation of the Stargardt disease gene (ABCR) in age-related macular degeneration

Mutations and polymorphisms in the human peripherin-RDS gene and their involvement in inherited retinal degeneration

RDS/peripherin gene mutations are frequent causes of central retinal dystrophies.

Fine localisation of the gene for central areolar choroidal dystrophy on chromosome 17p.

Dominantly inherited drusen of Bruch's membrane

Further evidence for an association of ABCR alleles with age-related macular degeneration. The International ABCR Screening Consortium.

A comprehensive survey of sequence variation in the ABCA4 (ABCR) gene in Stargardt disease and age-related macular degeneration.

A twin study on age-related macular degeneration

ATP binding cassette transporter retina genotypes and age related macular degeneration: an analysis on exudative non-familial Japanese patients.

P304

91-96

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

P31

scholarly article

P356

10.1136/BJO.86.1.91

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

P407

P433

1

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

P478

86

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

P577

2002-01-01T00:00:00Z

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

P5875

277397975

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

P698

11801511

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

P932

1770981

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