Variants in CIB2 cause DFNB48 and not USH1J-Reference-Cited by-同舟云学术

Variants in CIB2 cause DFNB48 and not USH1J

Published:2018-02-12 Issue:4 Volume:93 Page:812-821
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:Clin Genet

Author:

Booth K.T.¹²^ORCID,Kahrizi K.³^ORCID,Babanejad M.³^ORCID,Daghagh H.³,Bademci G.⁴^ORCID,Arzhangi S.³,Zareabdollahi D.³,Duman D.⁵^ORCID,El-Amraoui A.⁶^ORCID,Tekin M.⁷^ORCID,Najmabadi H.³^ORCID,Azaiez H.¹^ORCID,Smith R.J.¹^ORCID

Affiliation:

1. Department of Otolaryngology, Head and Neck Surgery, Molecular Otolaryngology and Renal Research Laboratories; University of Iowa; Iowa City, IA, USA

2. Interdisciplinary Graduate Program in Molecular Medicine; Carver College of Medicine, University of Iowa; Iowa City, IA, USA

3. Genetics Research Center; University of Social Welfare and Rehabilitation Sciences; Tehran Iran

4. John P. Hussman Institute for Human Genomics; University of Miami Miller School of Medicine; Miami, FL, USA

5. Division of Pediatric Genetics; Ankara University School of Medicine; Ankara Turkey

6. Institut Pasteur; Génétique et Physiologie de l'Audition; Paris France

7. John P. Hussman Institute for Human Genomics, Dr. John T. Macdonald Foundation Department of Human Genetics, Department of Otolaryngology; University of Miami Miller School of Medicine; Miami, FL, USA

Funder

National Institute on Deafness and Other Communication Disorders

Iran National Science Foundation

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/cge.13170/fullpdf

Reference40 articles.

1. Genetic epidemiology of hearing impairment;Morton;Ann N Y Acad Sci,1991

2. Lentz J Keats BJ 1993 http://www.ncbi.nlm.nih.gov/pubmed/20301442