Genomic testing in patients with suspected Familial Chylomicronaemia Syndrome (FCS) and evaluation of the FCS clinical scoring tool

• J.C. Evans,
• P. Downie,
• G. Bayly,
• H. Soran,
• E. Price,
• R. Butler,
• M. Williams

Affiliations

J.C. Evans

Corresponding author.; Bristol Genetics Laboratory, South West Genomics Laboratory Hub, Bristol, United Kingdom

P. Downie

University Hospitals of Bristol NHS Foundation Trust, Bristol, United Kingdom

G. Bayly

University Hospitals of Bristol NHS Foundation Trust, Bristol, United Kingdom

H. Soran

Faculty of Biology, Medicine and Health, University of Manchester, Manchester, United Kingdom; Cardiovascular Trials Unit, Manchester University NHS Foundation Trust, Manchester, United Kingdom

E. Price

Bristol Genetics Laboratory, South West Genomics Laboratory Hub, Bristol, United Kingdom; Neuro-Epigenetics Research Group, Bristol Medical School, University of Bristol, Bristol, United Kingdom

R. Butler

Bristol Genetics Laboratory, South West Genomics Laboratory Hub, Bristol, United Kingdom

M. Williams

Bristol Genetics Laboratory, South West Genomics Laboratory Hub, Bristol, United Kingdom