Identification of mutations in the repeated part of the autosomal dominant polycystic kidney disease type 1 gene, PKD1, by long-range PCR

American Journal of Human Genetics

Volumn 65, Issue 1, 1999, Pages 39-49

  Thomas, Ruth ^a   McConnell, Robert ^a   Whittacker, Jo ^a   Kirkpatrick, Peter ^a   Bradley, John ^a   Sandford, Richard ^a  

^a ADDENBROOKE S HOSPITAL   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

CELL ADHESION MOLECULE; CELL SURFACE RECEPTOR; GENE PRODUCT; POLYCYSTIN;

ARTICLE; AUTOSOMAL DOMINANT DISORDER; CLINICAL ARTICLE; EXON; GENE DELETION; GENE DUPLICATION; GENE INSERTION; GENE MUTATION; GENETIC POLYMORPHISM; GENETIC SCREENING; HUMAN; INTRON; KIDNEY POLYCYSTIC DISEASE; NUCLEIC ACID BASE SUBSTITUTION; NUCLEOTIDE SEQUENCE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; PROTEIN DOMAIN; SEQUENCE ANALYSIS;

EID: 0033365404     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/302460     Document Type: Article

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