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Identification of molecular defects in portuguese patients with familial hypercholesterolaemia

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📜 SIMILAR VOLUMES

YI-802 MOLECULAR CHARACTERIZATION OF FAM

✍ Medeiros, A.M.; Alves, A.C.; Silva, S.; Bourbon, M. 📂 Article 📅 2007 🏛 Elsevier Science 🌐 English ⚖ 66 KB

The molecular basis of familial hypercho

✍ M. Mert Sözen; Ros Whittall; Cihan Öner; Ayşegül Tokatlı; H. Serap Kalkanoğlu; A 📂 Article 📅 2005 🏛 Elsevier Science 🌐 English ⚖ 262 KB

Absence of familial defective apolipopro

✍ Atsushi Nohara; Kunimasa Yagi; Akihiro Inazu; Kouji Kajinami; Junji Koizumi; Hir 📂 Article 📅 1995 🏛 The Lancet 🌐 English ⚖ 163 KB

Identification of new mutations in the l

✍ J. Webb; X-M. Sun; B.L. Knight; A.K. Soutar 📂 Article 📅 1993 🏛 Elsevier Science 🌐 English ⚖ 116 KB

Rapid testing for three mutations causin

✍ Philippa J. Talmud; Owen J. Tamplin; Karen Heath; Dairiena Gaffney; Ian N.M. Day 📂 Article 📅 1996 🏛 Elsevier Science 🌐 English ⚖ 259 KB

YI-800 FUNCTIONAL CHARACTERIZATION OF PO

✍ Silva, S.; Patel, D.; Bourbon, M.; Soutar, A.K. 📂 Article 📅 2007 🏛 Elsevier Science 🌐 English ⚖ 68 KB