An axonal Charcot–Marie–Tooth disease associated with a homozygous GDAP1 gene mutation in two siblings from Bangladesh: a less severe phenotype

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作者：
Catarina Correia Rodrigues
Miguel Oliveira Santos
机构：
[1] Hospital de Santa Maria,Department of Neurosciences and Mental Health
[2] Centro Hospitalar Universitário Lisboa Norte,Institute of Physiology
[3] Instituto de Medicina Molecular,undefined
[4] Faculdade de Medicina da Universidade de Lisboa,undefined
来源：
Acta Neurologica Belgica | 2022年 / 122卷
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页码：841 / 842
页数：1
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