Gene table: search width pubmed_id = 22961002


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

protein
All allelic disease phenotypes - locus/disease symbols
Neuromyotonia and axonal neuropathy, autosomal recessive - (AR)
14.92
22961002
HINT1 (5q23.3)
Histidine triad nucleotide binding protein 1
* Neuromyotonia and axonal neuropathy, autosomal recessive - NMAN
* Neuronopathy, Distal hereditary motor related to HINT1