Targeted genomic enrichment and massively parallel sequencing identifies novel nonsyndromic hearing impairment pathogenic variants in Cameroonian families-Reference-Cited by-同舟云学术

Targeted genomic enrichment and massively parallel sequencing identifies novel nonsyndromic hearing impairment pathogenic variants in Cameroonian families

Published:2016-06-01 Issue:3 Volume:90 Page:288-290
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:Clin Genet

Author:

Lebeko K.¹,Sloan-Heggen C. M.²,Noubiap J. J. N.³,Dandara C.¹,Kolbe D. L.²,Ephraim S. S.²,Booth K. T.²,Azaiez H.²,Santos-Cortez R. L. P.⁴,Leal S. M.⁴,Smith R. J. H.²,Wonkam A.¹³

Affiliation:

1. Division of Human Genetics, Department of Pathology; Faculty of Health Sciences University of Cape Town; Cape Town South Africa

2. Department of Otolaryngology; Molecular Otolaryngology and Renal Research Laboratories, The University of Iowa; Iowa City IA USA

3. Department of Medicine; Faculty of Health Sciences University of Cape Town; Cape Town South Africa

4. Center for Statistical Genetics, Department of Molecular and Human Genetics; Baylor College of Medicine; Houston TX USA

Funder

Medical Research Counsel

National Research Foundation

National Health laboratory Services (NHLS)

NIH-National Institute of Deafness and other Communication Disorders

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference11 articles.

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2. Comprehensive genetic testing for hereditary hearing loss using massively parallel sequencing;Shearer;Proc Natl Acad Sci U S A,2010

3. Aetiology of childhood hearing loss in Cameroon (sub-Saharan Africa);Wonkam;Eur J Med Genet,2013

4. ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data;Wang;Nucleic Acids Res,2010

5. Comprehensive genetic testing in the clinical evaluation of 1119 patients with hearing loss;Sloan-Heggen;Hum Genet,2016

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