Period of time: 2003年2期
Publisher: Elsevier
Founded in: 1967
Total resources: 50
ISSN: 1096-7192
Subject: R3 Basic Medical
Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.
Molecular Genetics and Metabolism,volume 79,issue 2
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Regulation of the mitochondrial ATP-synthase in health and disease
Molecular Genetics and Metabolism,volume 79,issue 2 , Vol. 79, Iss. 2, 2003-06 , pp.By Rafi M.A., Coppola S., Liu S.L., Rao H.Z., Wenger D.A. in (2003)
Molecular Genetics and Metabolism,volume 79,issue 2 , Vol. 79, Iss. 2, 2003-06 , pp.By Coulter-Mackie M.B., Gagnier L. in (2003)
Molecular Genetics and Metabolism,volume 79,issue 2 , Vol. 79, Iss. 2, 2003-06 , pp.Mutation analysis of feline Niemann-Pick C1 disease
By Somers K.L., Royals M.A., Carstea E.D., Rafi M.A., Wenger D.A., Thrall M.A. in (2003)
Molecular Genetics and Metabolism,volume 79,issue 2 , Vol. 79, Iss. 2, 2003-06 , pp.By Tayebi N., Walker J., Stubblefield B., Orvisky E., LaMarca M.E., Wong K., Rosenbaum H., Schiffmann R., Bembi B., Sidransky E. in (2003)
Molecular Genetics and Metabolism,volume 79,issue 2 , Vol. 79, Iss. 2, 2003-06 , pp.Large neutral amino acid therapy and phenylketonuria: a promising approach to treatment
By Koch R., Moseley K.D., Yano S., Nelson M., Moats R.A. in (2003)
Molecular Genetics and Metabolism,volume 79,issue 2 , Vol. 79, Iss. 2, 2003-06 , pp.Optimal dietary therapy of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency
By Gillingham M.B., Connor W.E., Matern D., Rinaldo P., Burlingame T., Meeuws K., Harding C.O. in (2003)
Molecular Genetics and Metabolism,volume 79,issue 2 , Vol. 79, Iss. 2, 2003-06 , pp.A splice junction mutation in muscle carnitine palmitoyltransferase II deficiency
By Deschauer M., Chrzanowska-Lightowlers Z.M.A., Biekmann E., Pourfarzam M., Taylor R.W., Turnbull D.M., Zierz S. in (2003)
Molecular Genetics and Metabolism,volume 79,issue 2 , Vol. 79, Iss. 2, 2003-06 , pp.Analysis of the human folate receptor gene for an association with neural tube defects
By O'Leary V.B., Mills J.L., Kirke P.N., Parle-McDermott A., Swanson D.A., Weiler A., Pangilinan F., Conley M., Molloy A.M., Lynch M., Cox C., Scott J.M., Brody L.C. in (2003)
Molecular Genetics and Metabolism,volume 79,issue 2 , Vol. 79, Iss. 2, 2003-06 , pp.By Vlangos C.N., Yim D.K.C., Elsea S.H. in (2003)
Molecular Genetics and Metabolism,volume 79,issue 2 , Vol. 79, Iss. 2, 2003-06 , pp.