Gene table: search width pubmed_id = 32954258


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

protein
All allelic disease phenotypes - locus/disease symbols
Charcot-Marie-Tooth disease, axonal - (AR)
14.102
32954258
MCM3AP (21q22.3)
Minichromosome maintenance 3-associated protein
* Peripheral neuropathy, autosomal recessive, with or without impaired intellectual development - PNRIID
* Charcot-Marie-Tooth disease, axonal