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Connexin 26 (GJB2) mutations in the Turkish population: implications for the origin and high frequency of the 35delG mutation in Caucasians

Author
TEKIN, Mustafa1 2 ; AKAR, Nejat2 ; CIN, Sükrü2 ; BLANTON, Susan H1 3 ; XIA JUAN XIA1 ; XUE ZHONG LIU1 ; NANCE, Walter E1 ; PANDYA, Arti1
[1] Department of Human Genetics, Medical College of Virginia/Virginia Commonwealth University, 1101 East Marshall Street, PO Box 980033, Richmond, VA 23298-0033, United States
[2] Department of Pediatrics, Ankara University School of Medicine, Ankara, Turkey
[3] Department of Pediatrics, University of Virginia, Charlottesville, Va., United States
Source

Human genetics. 2001, Vol 108, Num 5, pp 385-389 ; ref : 9 ref

CODEN
HUGEDQ
ISSN
0340-6717
Scientific domain
Biotechnology; Genetics
Publisher
Springer, Berlin / Springer, Heidelberg / Springer, New York, NY
Publication country
Germany
Document type
Article
Language
English
Keyword (fr)
Chromosome Connexine Etude familiale Gène Homme Marqueur génétique Mutation Surdité Polymorphisme mononucléotide
Keyword (en)
Chromosome Connexin Family study Gene Human Genetic marker Mutation Hearing loss
Keyword (es)
Cromosoma Connexina Estudio familiar Gen Hombre Marcador genético Mutación Sordera
Classification
Pascal
002 Biological and medical sciences / 002B Medical sciences / 002B10 Otorhinolaryngology. Stomatology / 002B10D Ear, auditive nerve, cochleovestibular tract, facial nerve: diseases, semeiology / 002B10D02 Non tumoral diseases

Discipline
Otorhinolaryngology. Stomatology
Origin
Inist-CNRS
Database
PASCAL
INIST identifier
1039969

Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS

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