Identifying pathogenic genetic background of simplex or multiplex retinitis pigmentosa patients: a large scale mutation screening study-Reference-Cited by-同舟云学术

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Identifying pathogenic genetic background of simplex or multiplex retinitis pigmentosa patients: a large scale mutation screening study

Published:2008-05-07 Issue:7 Volume:45 Page:465-472
ISSN:1468-6244
Container-title:Journal of Medical Genetics
language:en
Short-container-title:Journal of Medical Genetics

Author:

Jin Z-B,Mandai M,Yokota T,Higuchi K,Ohmori K,Ohtsuki F,Takakura S,Itabashi T,Wada Y,Akimoto M,Ooto S,Suzuki T,Hirami Y,Ikeda H,Kawagoe N,Oishi A,Ichiyama S,Takahashi M,Yoshimura N,Kosugi S

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Cited by 64 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

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3. Transcriptional precision in photoreceptor development and diseases – Lessons from 25 years of CRX research;Frontiers in Cellular Neuroscience;2024-02-13

4. Phenotypic and Genetic Alterations in Adult-Onset Cone and Cone-Rod Dystrophy;Ophthalmic Research;2023-12-13

5. IMPDH1 -associated autosomal dominant retinitis pigmentosa: natural history of novel variant Lys314Gln and a comprehensive literature search;Ophthalmic Genetics;2023-05-31

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