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

Research output: Contribution to journal › Review article › peer-review

7 Citations (Scopus)

Original language	English
Pages (from-to)	137-149
Number of pages	13
Journal	Advances in Experimental Medicine and Biology
Volume	201
DOIs	https://doi.org/10.1007/978-1-4684-1262-8_13
Publication status	Published - 1986

ASJC Scopus Subject Areas

General Biochemistry,Genetics and Molecular Biology

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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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AU - Forte, T. M.

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AU - Ginsberg, H. N.

PY - 1986

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

ASJC Scopus Subject Areas

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