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slc26a4
- The SLC26A4 gene provides instructions for making a protein called pendrin. This protein transports negatively charged particles (ions), including chloride, ...
- ... from birth (congenital hearing loss). Mutations in the SLC26A4 gene cause about half of all cases of Pendred syndrome. The SLC26A4 gene provides instructions for making a protein called ...
- Thyroid Diseases/Related Issues ... Thyroid Diseases ... Hearing Problems in Children/Specifics ... Hearing Problems in Children ... National Institute on Deafness and Other ...
- ... syndrome (CDH23 and MYO7A, among others), Pendred syndrome (SLC26A4), Wolfram syndrome (WFS1), and Stickler syndrome (COL11A2). It ... GJB6 KCNQ4 MT-TS1 MYH9 MYO7A POU3F4 PRPS1 SLC26A4 STRC TBC1D24 TECTA WFS1 mitochondrial dna Additional Information ...
- Enlarged Vestibular Aqueducts and Childhood Hearing Loss
(National Institute on Deafness and Other Communication Disorders)
Hearing Problems in Children/Specifics ... Hearing Problems in Children ... Ear Disorders/Children ... Ear Disorders ... National Institute on Deafness and Other Communication ... - Enlarged Vestibular Aqueduct (EVA) (Vestibular Disorders Association)Enlarged Vestibular Aqueduct is a condition caused by a malformation in the inner ear that leads to loss of hearing and vestibular function. ... Dizziness ...
- ... in thyroid hormone production). FOXP3 HLA-DRB1 PTPN22 SLC26A4 TG Additional Information from NCBI Gene: CTLA4 The ...
- ... in syndromic forms of the disorder. DUOX2 PAX8 SLC26A4 SLC5A5 TG TPO TSHB TSHR Additional Information from ...
- ... hearing is unclear. APOE CDH23 KCNQ4 MTHFR MYO7A SLC26A4 mitochondrial dna Additional Information from NCBI Gene: EDN1 ...
- ... Usami S. Ethnic-specific spectrum of GJB2 and SLC26A4 mutations: their origin and a literature review. Ann ...