Gene table: search width pubmed_id = 33559681


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Disease phenotype
Item
in
this
table
Key
references
Gene symbol (chromosome)

protein
All allelic disease phenotypes - locus/disease symbols
Neuropathy, hereditary motor, autosomal recessive 7 - (AR)
12.19
33459760
33559681
VWA1 (1p36.33)
Von Willebrand factor A domain-containing protein 1
* Neuropathy, hereditary motor, with myopathic features - HMNMYO