A complex phenotype in a child with familial HDL deficiency due to a novel frameshift mutation in APOA1 gene (apoA-I Guastalla )-Reference-Cited by-同舟云学术

A complex phenotype in a child with familial HDL deficiency due to a novel frameshift mutation in APOA1 gene (apoA-I Guastalla )

Published:2015-11 Issue:6 Volume:9 Page:837-846
ISSN:1933-2874
Container-title:Journal of Clinical Lipidology
language:en
Short-container-title:Journal of Clinical Lipidology

Author:

Pisciotta Livia,Vitali Cecilia,Favari Elda,Fossa Paola,Adorni Maria Pia,Leone Daniela,Artom Nathan,Fresa Raffaele,Calabresi Laura,Calandra Sebastiano,Bertolini Stefano^ORCID

Publisher

Elsevier BV

Subject

Cardiology and Cardiovascular Medicine,Nutrition and Dietetics,Endocrinology, Diabetes and Metabolism,Internal Medicine

Reference43 articles.

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5. Italian cross-sectional growth charts for height, weight and BMI (2 to 20 yr);Cacciari;J Endocrinol Invest,2006

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