Identification of novel mutations in the SEMA4A gene associated with retinal degenerative diseases-Reference-Cited by-同舟云学术

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Identification of novel mutations in the SEMA4A gene associated with retinal degenerative diseases

Published:2005-09-09 Issue:4 Volume:43 Page:378-381
ISSN:1468-6244
Container-title:Journal of Medical Genetics
language:en
Short-container-title:Journal of Medical Genetics

Author:

Abid A

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

1. A systematic review of inherited retinal dystrophies in Pakistan: updates from 1999 to April 2023;BMC Ophthalmology;2024-02-05

2. Four different gene-related cone–rod dystrophy: clinical and genetic findings in six Chinese families with diverse modes of inheritance;Frontiers in Genetics;2023-11-02

3. A systematic review of inherited retinal dystrophies in Pakistan: Updates from 1999 to April 2023;2023-06-26

4. Modulating antioxidant systems as a therapeutic approach to retinal degeneration;Redox Biology;2022-11

5. Retinitis Pigmentosa'nın Genetik ve Klinik Değerlendirilmesi;Journal of Contemporary Medicine;2022-09-30

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