Mutational Spectrum ofMYO15Aand the Molecular Mechanisms of DFNB3 Human Deafness-Reference-Cited by-同舟云学术

Mutational Spectrum ofMYO15Aand the Molecular Mechanisms of DFNB3 Human Deafness

Published:2016-08-21 Issue:10 Volume:37 Page:991-1003
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Human Mutation

Author:

Rehman Atteeq U.¹,Bird Jonathan E.¹,Faridi Rabia¹²,Shahzad Mohsin³,Shah Sujay¹,Lee Kwanghyuk⁴,Khan Shaheen N.²,Imtiaz Ayesha¹,Ahmed Zubair M.³,Riazuddin Saima³,Santos-Cortez Regie Lyn P.⁴,Ahmad Wasim⁵,Leal Suzanne M.⁴,Riazuddin Sheikh⁶,Friedman Thomas B.¹

Affiliation:

1. Laboratory of Molecular Genetics; National Institute on Deafness and Other Communication Disorders; National Institutes of Health; Bethesda Maryland 20892

2. Centre of Excellence in Molecular Biology; University of the Punjab; Lahore 54550 Pakistan

3. Department of Otorhinolaryngology Head & Neck Surgery; School of Medicine; University of Maryland; Baltimore Maryland 21201

4. Center for Statistical Genetics; Department of Molecular and Human Genetics; Baylor College of Medicine; Houston Texas 77030

5. Department of Biochemistry; Faculty of Biological Sciences; Quaid-i-Azam University; Islamabad 45320 Pakistan

6. Allama Iqbal Medical Research Centre; Jinnah Hospital Complex; University of Health Sciences; Lahore 54550 Pakistan

Funder

National Institutes of Health

Higher Education Commission, Pakistan

National Institute on Deafness and Other Communication Disorders

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference106 articles.

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3. Diversity of the causal genes in hearing impaired algerian individuals identified by whole exome sequencing;Ammar-Khodja;Mol Genet Genomic Med,2015

4. The motor and tail regions of myosin xv are critical for normal structure and function of auditory and vestibular hair cells;Anderson;Hum Mol Genet,2000

5. Tmc gene therapy restores auditory function in deaf mice;Askew;Sci Transl Med,2015

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