Gene table: search width pubmed_id = 8957026


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

protein
All allelic disease phenotypes - locus/disease symbols
Myasthenic syndrome, congenital, 4C, associated with acetylcholine receptor deficiency - (AR)
11.11
8957026
9158150
CHRNE (17p13-p12)
Cholinergic receptor, nicotinic, epsilon
* Myasthenic syndrome, fast-channel congenital - FCCMS
* Myasthenic syndrome, slow-channel congenital - SCCMS
* Myasthenic syndrome, congenital, 4C, associated with acetylcholine receptor deficiency - CMS4C