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Keyword:
Compound heterozygous mutation
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Autosomal recessive spinocerebellar ataxia type 4 with a VPS13D mutation: A case report
1/12/2022 4:01:56 AM |
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Crumbs homolog 2 mutation in two siblings with steroid-resistant nephrotic syndrome: Two case reports
4/22/2021 12:14:42 PM |
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