Cystathionine ß-synthase mutations in homocystinuria

Authors :: Kraus, J.P.
Janosik, M.
Kozich, V.
Mandell, R.
Shih, V.
Sperando, M.P.
Sebastio, G.
Franchis, R. de
Andria, G.
Kluijtmans, L.A.J.
Blom, H.J.
Boers, G.H.J.
Gordon, R.B.
Kamoun, P.
Tsai, M.Y.
Kruger, W.D.
Koch, H.G.
Ohura, T.
Gaustadnes, M.
Source :: Human Mutation, 13, 362-375, Human Mutation, 13, pp. 362-375
Publication Year :: 1999
Abstract: Item does not contain fulltext 14 p.

Subjects :: Molecular genetic invest of cystathionine synthase deficiency as risk factor for vascular disease
diagnose en behandeling van milde vormen [Hyperhomocysteinemie]
diagnosis and treatment of mild abnormalities. [Hyperhomocysteinemia]
Moleculair genetisch onderzoek naar cystathionine synthase deficiëntie als risicofactor voor hart- en vaatziekten

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