نتائج البحث

Complete congenital stationary night blindness associated with a novel NYX variant (p.Asn216Lys) in middle-aged and older adult patients.

• Authors : Hayashi T; Department of Ophthalmology, The Jikei University School of Medicine, Tokyo, Japan.; Department of Ophthalmology, Katsushika Medical Center, The Jikei University School of Medicine, Tokyo, Japan.

Subjects: Mutation, Missense*; Eye Diseases, Hereditary/Eye Diseases, Hereditary/Eye Diseases, Hereditary/*genetics ; Genetic Diseases, X-Linked/Genetic Diseases, X-Linked/Genetic Diseases, X-Linked/*genetics Night blindness, congenital stationary

• Source: Ophthalmic genetics [Ophthalmic Genet] 2021 Aug; Vol. 42 (4), pp. 412-419. Date of Electronic Publication: 2021 Mar 26.Publisher: Informa Healthcare Country of Publication: England NLM ID: 9436057 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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