Gene table: search width pubmed_id = 32439808


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

protein
All allelic disease phenotypes - locus/disease symbols
Mitochondrial myopathy with lactic acidosis, cognitive impairment and autistic features - (XL)
16.83
32439808
APOO (Xp22.11)
Apolipoprotein O(M)
* Mitochondrial myopathy with lactic acidosis, cognitive impairment and autistic features