Identification of FH-causing variants in patients with clinical familial hypercholesterolaemia recruited into the 100,000 genome project: preliminary analysis
A. Rimbert,
M. Futema,
M. Williams,
E. Watson,
S.E. Humphries
Affiliations
A. Rimbert
l'institut du thorax, INSERM, CNRS, Univ Nantes, France
M. Futema
Centre for Heart Muscle Disease, Institute for Cardiovascular Science, UCL, London
M. Williams
Bristol Genetics Laboratory, North Bristol NHS Trust, UK
E. Watson
Bristol Genetics Laboratory, North Bristol NHS Trust, UK
S.E. Humphries
Corresponding author.; Centre for Cardiovascular Genetics, Institute for Cardiovascular Science, UCL, London
