Gene table: search width pubmed_id = 38960055


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

protein
All allelic disease phenotypes - locus/disease symbols
Sensory-motor neuropathy with oculofacial apraxia
12.48
38960055
COX18 (4q13.3)
Cytochrome c Oxidase Assembly Factor COX18(M)
* Sensory-motor neuropathy with oculofacial apraxia