All diseases

OMIM ID
610542
OMIM term:
MYASTHENIC SYNDROME, CONGENITAL, WITH TUBULAR AGGREGATES 1; CMSTA1
Alternative terms:

(∗) Location:
2p13.3  
(†) Associated OMIM genes:
GFPT1  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/8grqde0l