Gene table: search width pubmed_id = 21786366


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
Combined oxydative phosphorylation deficiency 9 - (AR)
10.35
21786366
MRPL3 (3q21-q23)
Mitochondrial ribosomal protein L3(M)
* Hypertrophic mitochondrial cardiomyopathy related to MRPL3