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Authors: PHAMDINH D BLANQUETGROSSARD F RESSOT C BRUZZONE R DAUTIGNY A
Citation: D. Phamdinh et al., 3 GENES, 4 DEMYELINATING PERIPHERAL NEUROPATHIES - FIRST GENOTYPE PHENOTYPE CORRELATIONS/, MS. Medecine sciences, 13(10), 1997, pp. 1113-1122

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
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