Molecular analysis of SLC26A4 gene in patients with nonsyndromic hearing loss and EVA: Identification of two novel mutations in Brazilian patients-Reference-Cited by-同舟云学术

Molecular analysis of SLC26A4 gene in patients with nonsyndromic hearing loss and EVA: Identification of two novel mutations in Brazilian patients

Published:2013-03 Issue:3 Volume:77 Page:410-413
ISSN:0165-5876
Container-title:International Journal of Pediatric Otorhinolaryngology
language:en
Short-container-title:International Journal of Pediatric Otorhinolaryngology

Author:

de Moraes Vanessa Cristine Sousa,dos Santos Nathalia Zocal Pereira,Ramos Priscila Zonzini,Svidnicki Maria Carolina Costa Melo,Castilho Arthur Menino,Sartorato Edi Lúcia

Publisher

Elsevier BV

Subject

Otorhinolaryngology,General Medicine,Pediatrics, Perinatology and Child Health

Reference24 articles.

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2. Association of congenital deafness with goiter: the nature of thyroid defect;Morgans;Lancet,1958

3. Association of congenital deafness with goiter (Pendred's syndrome): a study of 207 families;Fraser;Ann. Hum. Genet.,1965

4. Pendred syndrome is caused by mutations in a putative sulphate transporter gene (PDS);Everett;Nat. Genet.,1997

5. The Pendred syndrome gene encodes a chloride-iodide transport protein;Scott;Nat. Genet.,1999

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