A Gene for X-Linked Optic Atrophy Is Closely Linked to the Xp11.4-Xp11.2 Region of the X Chromosome

Author:

Assink Jacqueline J.M.,Tijmes Nel T.,Brink Jacoline B. ten,Oostra Roelof-Jan,Riemslag Frans C.,de Jong Paulus T.V.M.,Bergen Arthur A.B.

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Cited by 54 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. Inherited Optic Neuropathies;Reference Module in Neuroscience and Biobehavioral Psychology;2024

2. Variants in the WDR45 Gene Within the OPA-2 Locus Associate With Isolated X-Linked Optic Atrophy;Investigative Opthalmology & Visual Science;2023-10-11

3. Mitochondrial optic neuropathies;Mitochondrial Diseases;2023

4. Hereditary optic neuropathy associated with demyelinating diseases of the central nervous system;Zhurnal nevrologii i psikhiatrii im. S.S. Korsakova;2023

5. Ocular findings and genomics of X-linked recessive disorders: A review;Indian Journal of Ophthalmology;2022

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