Exome sequencing reveals neurodevelopmental genes in simplex consanguineous Iranian families with syndromic autism.
Ghasemi MR, Sadeghi H, Hashemi-Gorji F, Mirfakhraie R, Gupta V, Ben-Mahmoud A, Bagheri S, Razjouyan K, Salehpour S, Tonekaboni SH, Dianatpour M, Omrani D, Jang MH, Layman LC, Miryounesi M, Kim HG.
Ghasemi MR, et al. Among authors: razjouyan k.
BMC Med Genomics. 2024 Aug 5;17(1):196. doi: 10.1186/s12920-024-01969-6.
BMC Med Genomics. 2024.
PMID: 39103847
Free PMC article.