Erratum to "High incidence of the CFTR mutations 3272-26A → G and L927P in Belgian cystic fibrosis patients, and identification of three new CFTR mutations (186-2A → G, E588V, and 1671insTATCA)" [Journal of Cystic Fibrosis 6(2007)371-375] (DOI:10.1016/j.jcf.2006.10.013);High incidence of the CFTR mutations 3272-26A → G and L927P in Belgian cystic fibrosis patients, and identification of three new CFTR mutations (186-2A → G, E588V, and 1671insTATCA)

Journal of Cystic Fibrosis

Volumn 6, Issue 6, 2007, Pages 371-375

  Storm, Katrien ^a   Moens, Els ^a   Vits, Lieve ^a   De Vlieger, Haike ^a   Delaere, Gino ^a   D'Hollander, Maria ^a   Wuyts, Wim ^a   Biervliet, Martine ^a   Van Schil, Lutgardis ^b   Desager, Kristine ^a   Nöthen, Markus M ^a  

^a ANTWERP UNIVERSITY HOSPITAL   (Belgium)

^b Sint Vincentiusziekenhuis   (Belgium)

Author keywords

Antwerp; Belgian; CFTR; Cystic fibrosis; DGGE; Genotype phenotype

Indexed keywords

ADENINE; CYTOSINE; GENOMIC DNA; GLUTAMINE; GUANINE; LEUCINE; PROLINE; THYMINE; TRANSMEMBRANE CONDUCTANCE REGULATOR; VALINE;

ADULT; ARTICLE; BELGIUM; CYSTIC FIBROSIS; DENATURING GRADIENT GEL ELECTROPHORESIS; DNA SEQUENCE; FEMALE; FRAMESHIFT MUTATION; GENE FREQUENCY; GENE IDENTIFICATION; GENETIC SCREENING; HUMAN; INCIDENCE; MAJOR CLINICAL STUDY; MALE; MISSENSE MUTATION; NUCLEIC ACID BASE SUBSTITUTION; NUCLEOTIDE SEQUENCE; POPULATION RESEARCH;

EID: 35649024696     PISSN: 15691993     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jcf.2008.02.008     Document Type: Erratum

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