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Severe familial primary hypoalphalipoproteinemia in French Canadian kindred: no association with the apo A-I/C-III/A-IV and A-II gene loci, normal LCAT activity, normal triglyceride levels and lack of clinical manifestations of Tangier Disease

✍ Scribed by M. Marcil; B. Boucher; B.C. Solymos; J. Davignon; J. Frolich; J. Genest Jr


Book ID
118325592
Publisher
Elsevier Science
Year
1994
Tongue
English
Weight
309 KB
Volume
109
Category
Article
ISSN
0021-9150

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