Items where Author is "Nasrniya, S."
![]() | Up a level |
Group by: Item Type | No Grouping
Jump to: Article
Number of items: 2.
Article
(2025) Evaluation of pathogenic variant in WFS1 in a patient with Wolfram syndrome. Egyptian Journal of Medical Human Genetics. p. 8. ISSN 1110-8630
(2022) Whole-Exome Sequencing Identifies a Recurrent Small In-Frame Deletion in MYO15A Causing Autosomal Recessive Nonsyndromic Hearing Loss in 3 Iranian Pedigrees. Lab Med. pp. 111-122. ISSN 0007-5027