Gene table: search width pubmed_id = 24123876


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

protein
All allelic disease phenotypes - locus/disease symbols
Peripheral neuropathy, autosomal recessive, with or without impaired intellectual development - (AR)
12.109
24123876
28633435
MCM3AP (21q22.3)
Minichromosome maintenance 3-associated protein
* Peripheral neuropathy, autosomal recessive, with or without impaired intellectual development - PNRIID
* Charcot-Marie-Tooth disease, axonal