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A complex phenotype in a child with familial HDL deficiency due to a novel frameshift mutation in APOA1 gene (apoA-IGuastalla) |
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Titel: |
A complex phenotype in a child with familial HDL deficiency due to a novel frameshift mutation in APOA1 gene (apoA-IGuastalla) |
Auteur: |
Pisciotta, Livia Vitali, Cecilia Favari, Elda Fossa, Paola Adorni, Maria Pia Leone, Daniela Artom, Nathan Fresa, Raffaele Calabresi, Laura Calandra, Sebastiano Bertolini, Stefano |
Verschenen in: |
Journal of clinical lipidology |
Paginering: |
Jaargang 9 (2015) nr. 6 pagina's 10 p. |
Jaar: |
2015 |
Inhoud: |
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Uitgever: |
National Lipid Association |
Bronbestand: |
Elektronische Wetenschappelijke Tijdschriften |
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