Case Report: Chanarin-Dorfman Syndrome: A Novel Homozygous Mutation in ABHD5 Gene in a Chinese Case and Genotype-Phenotype Correlation Analysis

Overview of attention for article published in Frontiers in Genetics, March 2022

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New Research: Case Report: Chanarin-Dorfman Syndrome: A Novel Homozygous Mutation in ABHD5 Gene in a Chinese Case and Genotype-Phenotype Correlation Analysis: The Chanarin–Dorfman syndrome (CDS) is a rare, autosomal recessively inherited… https://t.co/UgKv

28 Mar 2022

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