Disease: Stuttering ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0038506
Disease: Stuttering
Stuttering 		0.040 GeneticVariation phenotype BEFREE 14 variations were found in the three genes 3 of which, including a novel variant within intronic region of GNPTG and a heterozygous 2-bp deletion in coding region of GNPTAB, co-segregated with stuttering in the families they were found. 29289611 2018
CUI: C0038506
Disease: Stuttering
Stuttering 		0.040 GeneticVariation phenotype BEFREE Our results revealed that the stuttering risk genes GNPTAB and NAGPA might also associate with developmental dyslexia in the Chinese population. 25643770 2015
CUI: C0038506
Disease: Stuttering
Stuttering 		0.040 GeneticVariation phenotype BEFREE Surprisingly, the first variant genes to be associated with stuttering are those encoding the lysosomal targeting system, GNPTAB, GNPTG, and NAGPA. 22884963 2012
CUI: C0038506
Disease: Stuttering
Stuttering 		0.040 GeneticVariation phenotype BEFREE This and three other mutations in GNPTAB occurred in unrelated subjects with stuttering but not in control subjects. 20147709 2010