Clinical syndrome and lipid metabolism in hereditary deficiency of apolipoproteins A-I and C-III, variant 1.

R. A. Norum; T. M. Forte; P. Alaupovic; H. N. Ginsberg

doi:10.1007/978-1-4684-1262-8_13

Clinical syndrome and lipid metabolism in hereditary deficiency of apolipoproteins A-I and C-III, variant 1.

R. A. Norum, T. M. Forte, P. Alaupovic, H. N. Ginsberg

Vagelos College of Physicians and Surgeons

Producción científica › revisión exhaustiva

7 Citas (Scopus)

Idioma original	English
Páginas (desde-hasta)	137-149
Número de páginas	13
Publicación	Advances in Experimental Medicine and Biology
Volumen	201
DOI	https://doi.org/10.1007/978-1-4684-1262-8_13
Estado	Published - 1986

ASJC Scopus Subject Areas

General Biochemistry,Genetics and Molecular Biology

Acceder al documento

10.1007/978-1-4684-1262-8_13

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Norum, R. A., Forte, T. M., Alaupovic, P., & Ginsberg, H. N. (1986). Clinical syndrome and lipid metabolism in hereditary deficiency of apolipoproteins A-I and C-III, variant 1. Advances in Experimental Medicine and Biology, 201, 137-149. https://doi.org/10.1007/978-1-4684-1262-8_13

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