All diseases

OMIM ID
609560
OMIM term:
MITOCHONDRIAL DNA DEPLETION SYNDROME 2 (MYOPATHIC TYPE); MTDPS2
Alternative terms:

(∗) Location:
16q21  
(†) Associated OMIM genes:
TK2  
(‡) Associated MGI genes:
Tk2  

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Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/39eklpnq