CFTR mutations in the Algerian population

Journal of Cystic Fibrosis

Volumn 7, Issue 1, 2008, Pages 54-59

  Loumi, O ^a   Ferec, C ^b   Mercier, B ^b   Creff, J ^b   Fercot, B ^b   Denine, R ^c   Grangaud, J P ^d  

^a UNIVERSITY OF SCIENCES AND TECHNOLOGY HOUARI BOUMEDIENE   (Algeria)

^b INSERM   (France)

^c Centre Hospitalier et Universitaire de Beni Messous Algiers   (Algeria)

^d Benyoucef Benkhedda   (Algeria)

Author keywords

Algeria; ARMS ; Cystic fibrosis; D HPLC; Denaturing gradient gel electrophoresis; Luminex ; Mutations; Polymorphisms; QMPSF

Indexed keywords

DNA; TRANSMEMBRANE CONDUCTANCE REGULATOR;

ALGERIA; ARTICLE; AZOOSPERMIA; CHILD; CHROMOSOME ANALYSIS; CLINICAL EVALUATION; CLINICAL FEATURE; CYSTIC FIBROSIS; DENATURING GRADIENT GEL ELECTROPHORESIS; DIAGNOSTIC ACCURACY; DNA SEQUENCE; EXON; FEMALE; FLUORESCENCE; GENE AMPLIFICATION; GENE DELETION; GENE DUPLICATION; GENE MUTATION; GENETIC ANALYSIS; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; HOMOZYGOSITY; HUMAN; MAJOR CLINICAL STUDY; MALE; MALE INFERTILITY; MULTIPLEX POLYMERASE CHAIN REACTION; NUCLEOTIDE SEQUENCE; POPULATION RESEARCH; RISK ASSESSMENT;

ADULT; ALGERIA; AZOOSPERMIA; CHILD; CHILD, PRESCHOOL; CYSTIC FIBROSIS; CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR; DNA MUTATIONAL ANALYSIS; FEMALE; HUMANS; MALE; MUTATION; POLYMORPHISM, SINGLE NUCLEOTIDE;

EID: 38049021626     PISSN: 15691993     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jcf.2007.04.004     Document Type: Article

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