Stuttering, Familial Persistent, 3 (STUT3)

External Ids:

OMIM® 57 614655 OMIM Phenotypic Series 57 PS184450

UMLS 71 C3553381

OMIM® : ⁵⁷ Stuttering is a disorder of the flow of speech characterized by involuntary repetitions or prolongations of sounds or syllables, and by interruptions of speech known as blocks (summary by Raza et al., 2010). For a general phenotypic description and a discussion of genetic heterogeneity of stuttering, see STUT1 (184450). (614655) (Updated 05-Mar-2021)

MalaCards based summary : Stuttering, Familial Persistent, 3, also known as stuttering, familial, persistent, type 3, is related to stuttering. An important gene associated with Stuttering, Familial Persistent, 3 is STUT3 (Stuttering, Familial Persistent, 3).

Clinical features from OMIM®:

614655 (Updated 05-Mar-2021)

Search Clinical Trials , NIH Clinical Center for Stuttering, Familial Persistent, 3

Search GEO for disease gene expression data for Stuttering, Familial Persistent, 3.