Population screening of F508del (DeltaF508), the most frequent mutation in the CFTR gene associated with cystic fibrosis in Argentina.

Human mutation

Volumn 18, Issue 2, 2001, Pages 167-

  Roque M ^a   Godoy, C P ^a   Castellanos, M ^a   Pusiol, E ^a   Mayorga, L S ^a  

^a FACULTAD DE CIENCIAS MÉDICAS   (Argentina)

Author keywords

[No Author keywords available]

Indexed keywords

CFTR PROTEIN, HUMAN; HETERODUPLEX; TRANSMEMBRANE CONDUCTANCE REGULATOR;

ARGENTINA; ARTICLE; BLOOD; CYSTIC FIBROSIS; EXON; GENE DELETION; GENE FREQUENCY; GENETIC SCREENING; GENETICS; HETEROZYGOTE; HUMAN; NUCLEOTIDE SEQUENCE; POLYMERASE CHAIN REACTION;

ARGENTINA; BASE SEQUENCE; CYSTIC FIBROSIS; CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR; EXONS; GENE FREQUENCY; GENETIC SCREENING; HETEROZYGOTE; HUMANS; NUCLEIC ACID HETERODUPLEXES; POLYMERASE CHAIN REACTION; SEQUENCE DELETION;

EID: 18044403553     PISSN: None     EISSN: 10981004     Source Type: Journal    
DOI: None     Document Type: Article

References (0)