An α-tectorin gene defect causes a newly identified autosomal recessive form of sensorineural pre-lingual non-syndromic deafness, DFNB21

Human Molecular Genetics

Volumn 8, Issue 3, 1999, Pages 409-412

  Mustapha, Mirna ^a,b   Weil, Dominique ^a   Chardenoux, Sébastien ^a   Elias, Sanaa ^c   El Zir, Elie ^d   Beckmann, Jacques S ^e   Loiselet, Jacques ^b   Petit, Christine ^a  

^a CNRS   (France)

^b SAINT JOSEPH UNIVERSITY   (Lebanon)

^c Nini Hospital   (Lebanon)

^d Sacre Coeur Hospital Baabda   (Lebanon)

^e GÉNÉTHON   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ALPHA TECTORIN; UNCLASSIFIED DRUG;

AMINO ACID SEQUENCE; ARTICLE; AUTOSOMAL RECESSIVE INHERITANCE; CHROMOSOME 11Q; CLINICAL ARTICLE; COCHLEA DUCT; CONSANGUINEOUS MARRIAGE; FEMALE; GENE LOCUS; GENE MAPPING; GENE SEQUENCE; GENETIC DISORDER; GENETIC LINKAGE; HUMAN; LEBANON; MALE; PERCEPTION DEAFNESS; PRIORITY JOURNAL;

EID: 0032977996     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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