Authors:
LATOUR P
FABREGUETTE A
RESSOT C
BLANQUETGROSSARD F
ANTOINE JC
CALVAS P
CHAPON F
CORBILLON E
OLLAGNON E
STURTZ F
BOUCHERAT M
CHAZOT G
DAUTIGNY A
PHAMDINH D
VANDENBERGHE A
Citation: P. Latour et al., NEW MUTATIONS IN THE X-LINKED FORM OF CHARCOT-MARIE-TOOTH DISEASE, European neurology, 37(1), 1997, pp. 38-42
Authors:
RESSOT C
LATOUR P
BLANQUETGROSSARD F
STURTZ F
DUTHEL S
BATTIN J
CORBILLON E
OLLAGNON E
SERVILLE F
VANDENBERGHE A
DAUTIGNY A
PHAMDINH D
Citation: C. Ressot et al., X-LINKED DOMINANT CHARCOT-MARIE-TOOTH NEUROPATHY (CMTX) - NEW MUTATIONS IN THE CONNEXIN32 GENE, Human genetics, 98(2), 1996, pp. 172-175
Authors:
BLANQUETGROSSARD F
PHAMDINH D
DAUTIGNY A
LATOUR P
BONNEBOUCHE C
CORBILLON E
CHAZOT G
VANDENBERGHE A
Citation: F. Blanquetgrossard et al., CHARCOT-MARIE-TOOTH TYPE 1B NEUROPATHY - 3RD MUTATION OF SERINE-63 CODON IN THE MAJOR PERIPHERAL MYELIN GLYCOPROTEIN P0 GENE, Clinical genetics, 48(6), 1995, pp. 281-283