Homozygosity Mapping Reveals Null Mutations in FAM161A as a Cause of Autosomal-Recessive Retinitis Pigmentosa-Reference-Cited by-同舟云学术

Homozygosity Mapping Reveals Null Mutations in FAM161A as a Cause of Autosomal-Recessive Retinitis Pigmentosa

Published:2010-09 Issue:3 Volume:87 Page:382-391
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Bandah-Rozenfeld Dikla,Mizrahi-Meissonnier Liliana,Farhy Chen,Obolensky Alexey,Chowers Itay,Pe'er Jacob,Merin Saul,Ben-Yosef Tamar,Ashery-Padan Ruth,Banin Eyal,Sharon Dror

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference30 articles.

1. Epidemiology of hereditary ocular disorders;Rosenberg;Dev. Ophthalmol.,2003

2. A study of retinitis pigmentosa in the City of Birmingham. II Clinical and genetic heterogeneity;Bundey;J. Med. Genet.,1984

3. Prevalence of retinitis pigmentosa in Maine;Bunker;Am. J. Ophthalmol.,1984

4. Retinitis pigmentosa;Hartong;Lancet,2006

5. Autosomal recessive retinitis pigmentosa locus RP28 maps between D2S1337 and D2S286 on chromosome 2p11-p15 in an Indian family;Gu;J. Med. Genet.,1999

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