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Authors: BRAUTIGAM C WEVERS RA JANSEN RJT SMEITINK JAM DERIJKVANANDEL JF GABREELS FJM HOFFMANN GF
Citation: C. Brautigam et al., BIOCHEMICAL HALLMARKS OF TYROSINE-HYDROXYLASE DEFICIENCY, Clinical chemistry, 44(9), 1998, pp. 1897-1904

Authors: JAEKEN J ARTIGAS J BARONE R FIUMARA A DEKONING TJ POLLTHE BT DERIJKVANANDEL JF HOFFMANN GF ASSMANN B MAYATEPEK E PINEDA M VILASECA MA SAUDUBRAY JM SCHLUTER B WEVERS R VANSCHAFTINGEN E
Citation: J. Jaeken et al., PHOSPHOMANNOMUTASE DEFICIENCY IS THE MAIN CAUSE OF CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME WITH TYPE-I ISOELECTROFOCUSING PATTERN OF SERUM SIALOTRANSFERRINS, Journal of inherited metabolic disease, 20(3), 1997, pp. 447-449

Authors: WEVERS RA DERIJKVANANDEL JF GABREELS FJM LUDECKE B BLAU N BARTHOLOME K
Citation: Ra. Wevers et al., A NEW CASE OF TYROSINE-HYDROXYLASE DEFICIENCY, Journal of neurochemistry, 66, 1996, pp. 27-27
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