Gene table: search width pubmed_id = 25574476


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

protein
All allelic disease phenotypes - locus/disease symbols
Infantile-onset multisystem disease with progressive muscle weakness - (AR)
16.72
25574476
PTRH2 (17q23.1)
Peptidyl-tRNA Hydrolase 2(M)
* Infantile-onset multisystem disease with progressive muscle weakness - IMNEPD