Mutation studies in the CFTR gene in asian Indian subjects with congenital bilateral absence of vas deferens: Report of two novel mutations and four novel variants

Genetic Testing and Molecular Biomarkers

Volumn 15, Issue 5, 2011, Pages 307-312

  Sachdeva, Kabir ^a   Saxena, Renu ^a   Majumdar, Abha ^b   Chadha, Sudhir ^b   Verma, Ishwar Chander ^a  

^a GURU GOBIND SINGH INDRAPRASTHA UNIVERSITY   (India)

^b SIR GANGA RAM HOSPITAL   (India)

Author keywords

[No Author keywords available]

Indexed keywords

TRANSMEMBRANE CONDUCTANCE REGULATOR;

ADULT; ALLELE; ARTICLE; CLINICAL ARTICLE; CONGENITAL BILATERAL ABSENCE OF VAS DEFERENS; CONTROLLED STUDY; CYSTIC FIBROSIS; DISEASE SEVERITY; DNA POLYMORPHISM; GENE MUTATION; GENE SEQUENCE; GENETIC VARIABILITY; HUMAN; INDIAN; MALE; MALE INFERTILITY; SINGLE STRAND CONFORMATION POLYMORPHISM;

ADULT; ASIAN CONTINENTAL ANCESTRY GROUP; CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR; DNA MUTATIONAL ANALYSIS; GENE FREQUENCY; GENETIC VARIATION; HUMANS; INDIA; INFERTILITY, MALE; MALE; MIDDLE AGED; MUTATION; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL; SEQUENCE ANALYSIS, DNA; VAS DEFERENS;

EID: 79956085448     PISSN: 19450265     EISSN: 19450257     Source Type: Journal    
DOI: 10.1089/gtmb.2010.0156     Document Type: Article

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