Recurrent and Private MYO15A Mutations Are Associated with Deafness in the Turkish Population-Reference-Cited by-同舟云学术

Recurrent and Private MYO15A Mutations Are Associated with Deafness in the Turkish Population

Published:2010-08 Issue:4 Volume:14 Page:543-550
ISSN:1945-0265
Container-title:Genetic Testing and Molecular Biomarkers
language:en
Short-container-title:Genetic Testing and Molecular Biomarkers

Author:

Cengiz F. Basak¹,Duman Duygu¹,Sırmacı Aslı²,Tokgöz-Yilmaz Suna¹,Erbek Seyra³,Öztürkmen-Akay Hatice⁴,İncesulu Armaḡan⁵,Edwards Yvonne J.K.²,Özdaḡ Hilal⁶,Liu Xue Z.⁷,Tekin Mustafa¹²

Affiliation:

1. Division of Genetics, Department of Pediatrics, Ankara University School of Medicine, Ankara, Turkey.

2. Dr. John T. Macdonald Department of Human Genetics and John P. Hussman Institute for Human Genomics, Miller School of Medicine, University of Miami, Miami, Florida.

3. Department of Otorhinolaryngology, Baskent University School of Medicine, Ankara, Turkey.

4. Department of Radiology, Private Veni Vidi Hospital, Diyarbakir, Turkey.

5. Department of Otorhinolaryngology, Eskisehir Osmangazi University School of Medicine, Eskisehir, Turkey.

6. Biotechnology Institute, Ankara University, Ankara, Turkey.

7. Department of Otolaryngology, Miller School of Medicine, University of Miami, Miami, Florida.

Publisher

Mary Ann Liebert Inc

Subject

Genetics (clinical),General Medicine

Link

http://www.liebertpub.com/doi/pdf/10.1089/gtmb.2010.0039

Reference33 articles.