| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5948077 | Atherosclerosis | 2012 | 9 Pages |
Abstract
⺠Phenotypic expression in Tunisian familial hypercholesterolemia varied widely. ⺠We identified a new putative loss of function mutation in PCSK9 gene: p.P174S. ⺠Variants of PCSK9 and APOE genes explain a part of the phenotypic variability.
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Authors
Afef Slimani, Awatef Jelassi, Imen Jguirim, Mohamed Najah, Lamia Rebhi, Asma Omezzine, Faouzi Maatouk, Khaldoun Ben Hamda, Maha Kacem, Jean-Pierre Rabès, Marianne Abifadel, Catherine Boileau, Mustapha Rouis, Mohamed Naceur Slimane, Mathilde Varret,