Contribution of connexin26 (GJB2) mutations and founder effect to non-syndromic hearing loss in India.

Journal of medical genetics

Volumn 40, Issue 5, 2003, Pages

  RamShankar, M ^a   Girirajan, S ^a   Dagan, O ^a   Ravi Shankar, H M ^a   Jalvi, R ^a   Rangasayee, R ^a   Avraham, K B ^a   Anand, A ^a  

^a JAWAHARLAL NEHRU CENTRE FOR ADVANCED SCIENTIFIC RESEARCH   (India)

Author keywords

[No Author keywords available]

Indexed keywords

CONNEXIN 26; GAP JUNCTION PROTEIN;

AMINO ACID SEQUENCE; ARTICLE; AUDIOLOGY; CHEMISTRY; CONSANGUINITY; FOUNDER EFFECT; GENE FREQUENCY; GENETIC POLYMORPHISM; GENETICS; GENOTYPE; HEARING LOSS; HUMAN; INDIA; MOLECULAR GENETICS; MUTATION; NUCLEOTIDE SEQUENCE; PHENOTYPE;

AMINO ACID SEQUENCE; AUDIOLOGY; CONNEXINS; CONSANGUINITY; DNA MUTATIONAL ANALYSIS; FOUNDER EFFECT; GENE FREQUENCY; GENOTYPE; HEARING LOSS; HUMANS; INDIA; MOLECULAR SEQUENCE DATA; MUTATION; PHENOTYPE; POLYMORPHISM, GENETIC;

MLCS; MLOWN;

EID: 0043280848     PISSN: None     EISSN: 14686244     Source Type: Journal    
DOI: 10.1136/jmg.40.5.e68     Document Type: Article

References (0)