Phenotypes of SLC26A4 gene mutations: Pendred syndrome and hypoacusis with enlarged vestibular aqueduct.

Neuro endocrinology letters

Volumn 29, Issue 1, 2008, Pages 29-36

  Maciaszczyk, Katarzyna ^a   Lewiński, Andrzej ^a  

^a MEDICAL UNIVERSITY OF LODZ   (Poland)

Author keywords

[No Author keywords available]

Indexed keywords

CARRIER PROTEIN; SLC26A4 PROTEIN, HUMAN; UNCLASSIFIED DRUG;

CONGENITAL MALFORMATION; GENETICS; HEARING LOSS; HUMAN; MUTATION; PHENOTYPE; REVIEW; SYNDROME; VESTIBULE AQUEDUCT;

HEARING LOSS; HUMANS; MEMBRANE TRANSPORT PROTEINS; MUTATION; PHENOTYPE; SYNDROME; VESTIBULAR AQUEDUCT;

EID: 42149141703     PISSN: 0172780X     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Review

References (51)