Six years' experience with LipidSeq: clinical and research learnings from a hybrid, targeted sequencing panel for dyslipidemias.
Bmc Medical Genomics
Dron, Jacqueline S JS; Wang, Jian J; McIntyre, Adam D AD; Iacocca, Michael A MA; Robinson, John F JF; Ban, Matthew R MR; Cao, Henian H; Hegele, Robert A RA
Publication Date: 2020-02-10
Variant appearance in text: APOA1: 178T>G; Ser60Ala
Genetic and secondary causes of severe HDL deficiency and cardiovascular disease.
Journal Of Lipid Research
Geller, Andrew S AS; Polisecki, Eliana Y EY; Diffenderfer, Margaret R MR; Asztalos, Bela F BF; Karathanasis, Sotirios K SK; Hegele, Robert A RA; Schaefer, Ernst J EJ
Amyloidogenicity and clinical phenotype associated with five novel mutations in apolipoprotein A-I.
The American Journal Of Pathology
Rowczenio, Dorota D; Dogan, Ahmet A; Theis, Jason D JD; Vrana, Julie A JA; Lachmann, Helen J HJ; Wechalekar, Ashutosh D AD; Gilbertson, Janet A JA; Hunt, Toby T; Gibbs, Simon D J SD; Sattianayagam, Prayman T PT; Pinney, Jenny H JH; Hawkins, Philip N PN; Gillmore, Julian D JD