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Results: 2

Authors: Cailloux, F Gauthier-Barichard, F Mimault, C Isabelle, V Courtois, V Giraud, G Dastugue, B Boespflug-Tanguy, O
Citation: F. Cailloux et al., Genotype-phenotype correlation in inherited brain myelination defects due to proteolipid protein gene mutations, EUR J HUM G, 8(11), 2000, pp. 837-845

Authors: Mimault, C Giraud, G Courtois, V Cailloux, F Boire, JY Dastugue, B Boespflug-Tanguy, O
Citation: C. Mimault et al., Proteolipoprotein gene analysis in 82 patients with sporadic Pelizaeus-Merzbacher disease: Duplications, the major cause of the disease, originate more frequently in male germ cells, but point mutations do not, AM J HU GEN, 65(2), 1999, pp. 360-369
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