A founder TMIE mutation is a frequent cause of hearing loss in southeastern Anatolia

Journal article

Peer reviewed

A SIRMAM, H OZTÜRKMEN-AKAY, S ERBEK, A INCESULU, D DUMAN, S TASIR-YILMAZ, H OZDAG and M TEKIN

Clinical genetics, Vol.75(6), pp.562-567

2009

PMID: 19438934

Abstract

Fundamental and applied biological sciences. Psychology

Human

General aspects. Genetic counseling

Otorhinolaryngology. Stomatology

Non tumoral diseases

Ear, auditive nerve, cochleovestibular tract, facial nerve: diseases, semeiology

Medical genetics

Biological and medical sciences

Molecular and cellular biology

Genetics of eukaryotes. Biological and molecular evolution

Medical sciences

Population genetics, reproduction patterns

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Collaboration types: Domestic collaboration; International collaboration
Citation topics: 1 Clinical & Life Sciences; 1.150 Hearing Loss; 1.150.421 Cochlea
Web Of Science research areas: Genetics & Heredity
ESI research areas: Clinical Medicine

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Source: InCites

Title: A founder TMIE mutation is a frequent cause of hearing loss in southeastern Anatolia
Creators: A SIRMAM - Division of Clinical Molecular Pathology and Genetics, Department of Pediatrics, Ankara University School of Medicine, Ankara, Turkey
H OZTÜRKMEN-AKAY - Department of Radiology, Dicle University School of Medicine, Diyarbakir, Turkey
S ERBEK - Department of Otorhinolaryngology, Başkent University School of Medicine, Konya, Turkey
A INCESULU - Department of Otorhinolaryngology, Eskişehir Osmangazi University School of Medicine, Eskişehir, Turkey
D DUMAN - Division of Clinical Molecular Pathology and Genetics, Department of Pediatrics, Ankara University School of Medicine, Ankara, Turkey
S TASIR-YILMAZ - Ankara University Biotechnology Institute, Ankara, Turkey
H OZDAG - Ankara University Biotechnology Institute, Ankara, Turkey
M TEKIN - Division of Clinical Molecular Pathology and Genetics, Department of Pediatrics, Ankara University School of Medicine, Ankara, Turkey
Publication Details: Clinical genetics, Vol.75(6), pp.562-567
Publisher: Wiley-Blackwell; Oxford
Academic Unit: Miller School of Medicine; UMMG Dept of Human Genetics - Clinical and Translational Genetics; UMMG Dept of Human Genetics (Dr. John T. Macdonald Foundation)
Language: English
Resource Type: Journal article
PMID: 19438934
Record Identifier: 991031577821002976