Unresolved questions regarding human hereditary deafness.

Rehman, A U; Friedman, T B; Griffith, A J

Rehman, A U; Friedman, T B; Griffith, A J.

Affiliation

Rehman AU; Laboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, MD, USA.
Friedman TB; Laboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, MD, USA.
Griffith AJ; Otolaryngology Branch, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, MD, USA.

Oral Dis ; 23(5): 551-558, 2017 Jul.

Article in En | MEDLINE | ID: mdl-27259978

Subject(s)

Carrier Proteins/genetics; Deafness/genetics; Goiter, Nodular/genetics; Gonadal Dysgenesis, 46,XX/genetics; Hearing Loss, Sensorineural/genetics; Craniofacial Abnormalities/genetics; Endopeptidase Clp/genetics; GTPase-Activating Proteins; Hand Deformities, Congenital/genetics; Humans; Intellectual Disability/genetics; Membrane Proteins; Membrane Transport Proteins/genetics; Nails, Malformed/genetics; Nerve Tissue Proteins; Sulfate Transporters

Key words

CLPP; SLC26A4; TBC1D24; Pendred syndrome; Perrault syndrome; enlarged vestibular aqueduct; hereditary deafness

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Carrier Proteins / Gonadal Dysgenesis, 46,XX / Deafness / Goiter, Nodular / Hearing Loss, Sensorineural Limits: Humans Language: En Journal: Oral Dis Journal subject: ODONTOLOGIA Year: 2017 Type: Article Affiliation country: United States

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