Linkage Study of Best‘s Vitelliform Macular Dystrophy (VMD2) in a Large North American Family-Reference-Cited by-同舟云学术

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Linkage Study of Best‘s Vitelliform Macular Dystrophy (VMD2) in a Large North American Family

Published:1996 Issue:4 Volume:46 Page:211-220
ISSN:1423-0062
Container-title:Human Heredity
language:en
Short-container-title:Hum Hered

Author:

Hou Yu-Chih,Richards Julia E.,Bingham Eve L.,Pawar Hemant,Scott Kathy,Segal Meridee,Lunetta Kathryn L.,Boehnke Michael,Sieving Paul A.

Publisher

S. Karger AG

Subject

Genetics (clinical),Genetics

Cited by 9 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Molecular Physiology of Bestrophins: Multifunctional Membrane Proteins Linked to Best Disease and Other Retinopathies;Physiological Reviews;2008-04

2. Mutation Analysis of the VMD2 Gene in Thai Families with Best Macular Dystrophy;Ophthalmic Genetics;2008-01

3. hUNC93B1: a novel human gene representing a new gene family and encoding an unc-93-like protein;Gene;2002-01

4. Best’s Macular Dystrophy;International Ophthalmology Clinics;2001

5. Mutations in the VMD2 gene are associated with juvenile-onset vitelliform macular dystrophy (Best disease) and adult vitelliform macular dystrophy but not age-related macular degeneration;European Journal of Human Genetics;2000-04

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