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
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| Description | scientific article published on 31 August 2020 |
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author: Pegah Ghandil Malihe Mohamadian |
| Publication date | August 31, 2020 |
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