Items where Author is "Sanati, M. H."

Up a level
Export as [feed] Atom [feed] RSS 1.0 [feed] RSS 2.0
Group by: Item Type | No Grouping
Jump to: Article
Number of items: 1.

Article

(2016) Screening of DFNB3 in Iranian families with autosomal recessive non-syndromic hearing loss reveals a novel pathogenic mutation in the MyTh4 domain of the MYO15A gene in a linked family. Iranian Journal of Basic Medical Sciences. pp. 772-778. ISSN 2008-3866

This list was generated on Thu Nov 21 17:45:14 2024 +0330.