A two-tier approach to mutation detection in the COL4A5 gene for Alport syndrome.

Human mutation

Volumn 27, Issue 10, 2006, Pages 1061-

  King, Kathy ^a   Flinter, Frances A ^a   Green, Peter M ^a  

^a KING'S COLLEGE LONDON   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

COL4A5 PROTEIN, HUMAN; COLLAGEN TYPE 4;

ARTICLE; EXON; FEMALE; FRAMESHIFT MUTATION; GENE DELETION; GENETICS; HUMAN; MALE; METHODOLOGY; MISSENSE MUTATION; MOLECULAR GENETICS; MUTATION; NEPHRITIS; NUCLEOTIDE SEQUENCE; PATHOLOGY;

BASE SEQUENCE; COLLAGEN TYPE IV; DNA MUTATIONAL ANALYSIS; EXONS; FEMALE; FRAMESHIFT MUTATION; HUMANS; MALE; MOLECULAR SEQUENCE DATA; MUTATION; MUTATION, MISSENSE; NEPHRITIS, HEREDITARY; SEQUENCE DELETION;

EID: 33749155626     PISSN: None     EISSN: 10981004     Source Type: Journal    
DOI: 10.1002/humu.9453     Document Type: Article

References (0)