Title : Molecular analysis and clinical diversity of distal hereditary motor neuropathy.

Pub. Date : 2020 Jul

PMID : 32298515






1 Functional Relationships(s)
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Sentence
Compound Name
Protein Name
Organism
1 Mutation in the HSPB1 gene was the most common cause of dHMN. dhmn heat shock protein family B (small) member 1 Homo sapiens