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The first report of two homozygous sequence variants in FKRP and SELENON genes associated with syndromic congenital muscular dystrophy in Iran: Further expansion of the clinical phenotypes
Mohamadian, Malihe, Naseri, Mohsen, Ghandil, Pegah, Bahrami, Afsane, Momen, Ali AkbarJournal:
The Journal of Gene Medicine
DOI:
10.1002/jgm.3265
Date:
August, 2020
File:
PDF, 1.34 MB
2020