CHARCOT-MARIE-TOOTH TYPE-1B NEUROPATHY - A MUTATION AT THE SINGLE GLYCOSYLATION SITE IN THE MAJOR PERIPHERAL MYELIN GLYCOPROTEIN-P0

BLANQUETGROSSARD E PHAMDINH D DAUTIGNY A LATOUR P BONNEBOUCHE C DIRAISON P CHAPON F CHAZOT G VANDENBERGHE A

E. Blanquetgrossard et al., CHARCOT-MARIE-TOOTH TYPE-1B NEUROPATHY - A MUTATION AT THE SINGLE GLYCOSYLATION SITE IN THE MAJOR PERIPHERAL MYELIN GLYCOPROTEIN-P0, Human mutation, 8(2), 1996, pp. 185-186

8

Genetics & Heredity

Human mutation → ACNP

10597794

8

2

1996

185 - 186

ISI

1059-7794(1996)8:2<185:CTN-AM>2.0.ZU;2-7