Gene table: search width pubmed_id = 29498452


Grey lines background indicate newly added items
Disease phenotype
Item
in
this
table
Key
references
Gene symbol (chromosome)

protein
All allelic disease phenotypes - locus/disease symbols
Congenital myopathy 20 - (AR)
3.16
29498452
RYR3 (15q13-q14)
Ryanodine receptor 3
* Myopathy with nemaline bodies