Mutations in theANGPTL3Gene and Familial Combined Hypolipidemia: A Clinical and Biochemical Characterization-Reference-Cited by-同舟云学术

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Mutations in theANGPTL3Gene and Familial Combined Hypolipidemia: A Clinical and Biochemical Characterization

Published:2012-07 Issue:7 Volume:97 Page:E1266-E1275
ISSN:0021-972X
Container-title:The Journal of Clinical Endocrinology & Metabolism
language:en
Short-container-title:The Journal of Clinical Endocrinology & Metabolism

Author:

Minicocci Ilenia,Montali Anna,Robciuc Marius Robert,Quagliarini Fabiana,Censi Vincenzo,Labbadia Giancarlo,Gabiati Claudia,Pigna Giovanni,Sepe Maria Laura,Pannozzo Fabio,Lütjohann Dieter,Fazio Sergio,Jauhiainen Matti,Ehnholm Christian,Arca Marcello

Publisher

The Endocrine Society

Subject

Biochemistry (medical),Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism

Cited by 134 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

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