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Kabuki Syndrome: Identification of Two Novel Variants in KMT2D and KDM6A.
Khodaeian M, Jafarinia E, Bitarafan F, Shafeii S, Almadani N, Daneshmand MA, Garshasbi M. Khodaeian M, et al. Among authors: garshasbi m. Mol Syndromol. 2021 Apr;12(2):118-126. doi: 10.1159/000513199. Epub 2021 Feb 17. Mol Syndromol. 2021. PMID: 34012382 Free PMC article.
Correction to: High genetic heterogeneity of leukodystrophies in Iranian children: the first report of Iranian Leukodystrophy Registry.
Ashrafi M, Kameli R, Hosseinpour S, Razmara E, Zamani Z, Rezaei Z, Mashayekhi R, Pak N, Barzegar M, Azizimalamiri R, Kashani MR, Khosroshahi N, Rasulinezhad M, Heidari M, Amanat M, Abdi A, Mohammadi B, Mohammadi M, Zamani GR, Badv RS, Omrani A, Nikbakht S, Bereshneh AH, Movahedinia M, Moghaddam HF, Ardakani HS, Akbari MG, Tousi MB, Shahi MV, Hosseini F, Amouzadeh MH, Hosseini SA, Nikkhah A, Khajeh A, Alizadeh H, Yarali B, Rohani M, Karimi P, Elahi HML, Hosseiny SMM, Sadeghzadeh MS, Mohebbi H, Moghadam MH, Aryan H, Vahidnezhad H, Soveizi M, Rabbani B, Rabbani A, Mahdieh N, Garshasbi M, Tavasoli AR. Ashrafi M, et al. Among authors: garshasbi m. Neurogenetics. 2023 Oct;24(4):317-318. doi: 10.1007/s10048-023-00733-9. Neurogenetics. 2023. PMID: 37668767 No abstract available.
Isolated Congenital Anosmia and CNGA2 Mutation.
Sailani MR, Jingga I, MirMazlomi SH, Bitarafan F, Bernstein JA, Snyder MP, Garshasbi M. Sailani MR, et al. Among authors: garshasbi m. Sci Rep. 2017 Jun 1;7(1):2667. doi: 10.1038/s41598-017-02947-y. Sci Rep. 2017. PMID: 28572688 Free PMC article.
148 results