The c.242G>A mutation in LRTOMT gene is responsible for a high prevalence of deafness in the Moroccan population.

Molecular biology reports

Volumn 39, Issue 12, 2012, Pages 11011-11016

  Charif, Majida ^a   Bounaceur, Safaa ^b   Abidi, Omar ^b   Nahili, Halima ^b   Rouba, Hassan ^b   Kandil, Mostafa ^b   Boulouiz, Redouane ^b   Barakat, Abdelhamid ^b  

^a Institut Pasteur du Maroc   (Morocco)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

LRTOMT1 PROTEIN, HUMAN; PROTEIN;

ARTICLE; FEMALE; GENETIC PREDISPOSITION; GENETICS; HEARING IMPAIRMENT; HUMAN; MALE; MOLECULAR GENETICS; MOROCCO; MUTATION; NUCLEOTIDE SEQUENCE; PEDIGREE; PERCEPTION DEAFNESS; PREVALENCE; SINGLE NUCLEOTIDE POLYMORPHISM;

BASE SEQUENCE; DEAFNESS; FEMALE; GENETIC PREDISPOSITION TO DISEASE; HEARING LOSS; HUMANS; MALE; MOLECULAR SEQUENCE DATA; MOROCCO; MUTATION; PEDIGREE; POLYMORPHISM, SINGLE NUCLEOTIDE; PREVALENCE; PROTEINS; SENSORINEURAL;

EID: 85027931058     PISSN: None     EISSN: 15734978     Source Type: Journal    
DOI: 10.1007/s11033-012-2003-3     Document Type: Article

References (0)