Gene table: search width pubmed_id = 10562302


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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, 2C, associated with acetylcholine receptor deficiency - (AR)
11.9
10562302
CHRNB1 (17p13.1)
Cholinergic receptor, nicotinic, beta 1 muscle
* Myasthenic syndrome, congenital, Ie, included - CMS1E
* Myasthenic syndrome, slow-channel congenital - SCCMS
* Myasthenic syndrome, congenital, 2B, Fast-channel - CMS2B
* Myasthenic syndrome, congenital, 2A, Slow-channel - CMS2A