A non-ancestralRPGR missense mutation in families with either recessive or semi-dominant X-linked retinitis pigmentosa-Reference-Cited by-同舟云学术

A non-ancestralRPGR missense mutation in families with either recessive or semi-dominant X-linked retinitis pigmentosa

Published:2007-06-01 Issue:11 Volume:143A Page:1150-1158
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Banin Eyal,Mizrahi-Meissonnier Liliana,Neis Ruhama,Silverstein Shira,Magyar István,Abeliovich Dvorah,Roepman Ronald,Berger Wolfgang,Rosenberg Thomas,Sharon Dror

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference37 articles.

1. X-linked Retinitis Pigmentosa:RPGRMutations in Most Families with Definite X Linkage and Clustering of Mutations in a Short Sequence Stretch of Exon ORF15

2. Retinal Function Abnormalities in Patients Treated With Vigabatrin

3. X chromosome inactivation patterns in Russell-Silver syndrome patients and their mothers

4. Electroretinographic Testing as an Aid in Detection of Carriers of X-Chromosome-Linked Retinitis Pigmentosa

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