Gene table: search width pubmed_id = 17033963


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 3 - (AR)
10.33
17033963
TSFM (12q14.1)
Ts translation elongation factor, mitochondrial(M)
* Mitochondrial hypertrophic cardiomyopathy related to TSFM - COXPD3