Rare nonconservative LRP6 mutations are associated with metabolic syndrome

Human Mutation

Volumn 34, Issue 9, 2013, Pages 1221-1225

  Singh, Rajvir ^a   Smith, Emily ^a   Fathzadeh, Mohsen ^a   Liu, Wenzhong ^a   Go, Gwang Woong ^a   Subrahmanyan, Lakshman ^a   Faramarzi, Saeed ^a   Mckenna, William ^a,b   Mani, Arya ^a  

^a YALE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b UNIVERSITY COLLEGE LONDON   (United Kingdom)

Author keywords

Coronary artery disease; LRP6; Metabolic syndrome; Mutation

Indexed keywords

ARGININE; LOW DENSITY LIPOPROTEIN RECEPTOR RELATED PROTEIN 6; WNT PROTEIN;

ADULT; ARTICLE; CONTROLLED STUDY; CORONARY ARTERY BYPASS GRAFT; CORONARY ARTERY DISEASE; EUROPEAN AMERICAN; FEMALE; GENETIC ASSOCIATION; GLYCOSYLATION; HEART INFARCTION; HUMAN; HYPERTENSION; LIGAND BINDING; LOSS OF FUNCTION MUTATION; MAJOR CLINICAL STUDY; MALE; METABOLIC SYNDROME X; MISSENSE MUTATION; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; SIGNAL TRANSDUCTION;

EID: 84881616727     PISSN: 10597794     EISSN: 10981004     Source Type: Journal    
DOI: 10.1002/humu.22360     Document Type: Article

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