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Mudd's disease (MAT I/III deficiency): a survey of data for..:
Chien, Yin-Hsiu
;
Abdenur, Jose E
;
Baronio, Federico
...
1750-1172. , 2015
Link:
https://dspace.library.uu.nl/handle/1874/332879
RT Journal T1
Mudd's disease (MAT I/III deficiency): a survey of data for MAT1A homozygotes and compound heterozygotes
UL https://suche.suub.uni-bremen.de/peid=base-ftunivutrecht:oai:dspace.library.uu.nl:1874_332879&Exemplar=1&LAN=DE A1 Chien, Yin-Hsiu A1 Abdenur, Jose E A1 Baronio, Federico A1 Bannick, Allison Anne A1 Corrales, Fernando A1 Couce, Maria A1 Donner, Markus G A1 Ficicioglu, Can A1 Freehauf, Cynthia A1 Frithiof, Deborah A1 Gotway, Garrett A1 Hirabayashi, Koichi A1 Hofstede, FC A1 Hoganson, George A1 Hwu, Wuh-Liang A1 James, Philip A1 Kim, Sook A1 Korman, Stanley H A1 Lachmann, Robin A1 Levy, Harvey A1 Lindner, Martin A1 Lykopoulou, Lilia A1 Mayatepek, Ertan A1 Muntau, Ania A1 Okano, Yoshiyuki A1 Raymond, Kimiyo A1 Rubio-Gozalbo, Estela A1 Scholl-Buergi, Sabine A1 Schulze, Andreas A1 Singh, Rani A1 Stabler, Sally A1 Stuy, Mary A1 Thomas, Janet A1 Wagner, Conrad A1 Wilson, William G A1 Wortmann, Saskia A1 Yamamoto, Shigenori A1 Pao, Maryland A1 Blom, Henk J YR 2015 K1 METHIONINE ADENOSYLTRANSFERASE-I/III K1 S-ADENOSYLMETHIONINE SYNTHETASE K1 PLASMA TOTAL HOMOCYSTEINE K1 BLOOD-BRAIN-BARRIER K1 CEREBROSPINAL-FLUID K1 PERSISTENT HYPERMETHIONINEMIA K1 DOMINANT INHERITANCE K1 MESSENGER-RNA K1 EXPRESSION K1 MUTATION K1 Journal Article K1 Research Support K1 N.I.H K1 Intramural K1 Non-U.S. Gov't K1 Review JF 1750-1172 LK http://dx.doi.org/https://dspace.library.uu.nl/handle/1874/332879 DO https://dspace.library.uu.nl/handle/1874/332879 SF ELIB - SuUB Bremen
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