FRMD7 Gene Alterations in a Pakistani Family Associated with Congenital Idiopathic Nystagmus

Congenital idiopathic nystagmus (CIN) is an oculomotor disorder characterized by repetitive and rapid involuntary movement of the eye that usually develops in the first six months after birth. Unlike other forms of nystagmus, CIN is widely associated with mutations in the FRMD7 gene. This study invo...

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Detalles Bibliográficos
Autores principales: Arshad, Muhammad Waqar, Shabbir, Muhammad Imran, Asif, Saaim, Shahzad, Mohsin, Leydier, Larissa, Rai, Sunil Kumar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9957179/
https://www.ncbi.nlm.nih.gov/pubmed/36833273
http://dx.doi.org/10.3390/genes14020346

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9957179/
https://www.ncbi.nlm.nih.gov/pubmed/36833273
http://dx.doi.org/10.3390/genes14020346

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