Novel human pathological mutations. Gene symbol: F13A1. Disease: Factor XIII Deficiency

Human Genetics

Volumn 127, Issue 1, 2010, Pages 115-116

  Anwar, Rashida ^a   Valleley, Elizabeth M A ^a   Trinh, Chi H ^a  

^a UNIVERSITY OF LEEDS   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ARGININE; BLOOD CLOTTING FACTOR 13; CARBONYL DERIVATIVE; GLUTAMINE; HYDROGEN; OXYGEN; BLOOD CLOTTING FACTOR 13A;

AMINO ACID SUBSTITUTION; ATOM; BLOOD CLOTTING FACTOR 13 DEFICIENCY; HYDROGEN BOND; MISSENSE MUTATION; NONSENSE MUTATION; NOTE; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; PROTEIN CONFORMATION; PROTEIN DOMAIN; PROTEIN INTERACTION; PROTEIN TERTIARY STRUCTURE; ARTICLE; CODON; GENETICS; HUMAN;

CODON; FACTOR XIII DEFICIENCY; FACTOR XIIIA; HUMANS; MUTATION, MISSENSE;

EID: 77449096069     PISSN: 03406717     EISSN: 14321203     Source Type: Journal    
DOI: None     Document Type: Note

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