All diseases

OMIM ID
184450
OMIM term:
STUTTERING, FAMILIAL PERSISTENT, 1; STUT1
Alternative terms:

(∗) Location:
18p11.3-p11.2  
(†) Associated OMIM genes:
(‡) Associated MGI genes:

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Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/ovb5f93c