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Keyword:
Congenital muscular dystrophy
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Congenital muscular dystrophy caused by beta1,3-N-acetylgalactosaminyltransferase 2 gene mutation: Two case reports
1/15/2022 12:57:35 PM |
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Homozygous deletion, c. 1114-1116del, in exon 8 of the CRPPA gene causes congenital muscular dystrophy in Chinese family: A case report
6/24/2021 7:26:33 AM |
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