Items where Author is "Pourahmadiyan, A."

Article

(2022) Next-generation sequencing reveals a novel pathogenic variant in the ATM gene. Int J Neurosci. pp. 558-562. ISSN 0020-7454

(2021) Next-generation sequencing reveals a novel pathogenic variant in the ATM gene. Int J Neurosci. pp. 1-5. ISSN 0020-7454

(2019) A pathogenic variant in SLC26A4 is associated with Pendred syndrome in a consanguineous Iranian family. Int J Audiol. pp. 1-7. ISSN 1708-8186 (Electronic) 1499-2027 (Linking)

(2017) A novel pathogenic variant in an Iranian Ataxia telangiectasia family revealed by next-generation sequencing followed by in silico analysis. Journal of the Neurological Sciences. pp. 212-216. ISSN 0022-510X

(2016) Genetic linkage analysis of DFNB40 and DFNB48 loci in families with autosomal recessive non-syndromic hearing loss (ARNSHL) from western provinces of Iran. Journal of Isfahan Medical School. ISSN 10277595 (ISSN)