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Identification of two rare APOE mutations associated with Familial Hypercholesterolaemia in the north of England
Identification of two rare APOE mutations associated with Familial Hypercholesterolaemia in the north of England
2016
C. McAnulty
S. Boras
Ann Curtis
R. Chaston
E. Stevenson
D. Bourn
S Fairgrieve
M. Anderson
M. Burns
R.D.G. Neely
Keywords:
Endocrinology
Internal medicine
Apolipoprotein E
Diabetes mellitus
Medicine
Correction
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