PHOSPHOMANNOMUTASE DEFICIENCY IS THE MAIN CAUSE OF CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME WITH TYPE-I ISOELECTROFOCUSING PATTERN OF SERUM SIALOTRANSFERRINS

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

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

14

Endocrynology & Metabolism","Genetics & Heredity

Journal of inherited metabolic disease → ACNP

01418955

20

3

1997

447 - 449

ISI

0141-8955(1997)20:3<447:PDITMC>2.0.ZU;2-I