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STUT3
MCID: STT036
MIFTS: 8
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Stuttering, Familial Persistent, 3 (STUT3)
Categories:
Genetic diseases
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OMIM
:
58
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)
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). |
Diseases in the Stuttering, Familial Persistent, 3 family:
Diseases related to Stuttering, Familial Persistent, 3 via text searches within MalaCards or GeneCards Suite gene sharing:
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Genes related to Stuttering, Familial Persistent, 3 (1 elite genes): - Elite gene
- Cancer Census gene in COSMIC
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Search
GEO
for disease gene expression data for Stuttering, Familial Persistent, 3.
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