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Authors: Matsumoto, N Tamura, S Moser, A Moser, HW Braverman, N Suzuki, Y Shimozawa, N Kondo, N Fujiki, Y
Citation: N. Matsumoto et al., The peroxin Pex6p gene is impaired in peroxisomal biogenesis disorders of complementation group 6, J HUM GENET, 46(5), 2001, pp. 273-277

Authors: Braverman, N Steel, G Lin, P Moser, A Moser, H Valle, D
Citation: N. Braverman et al., PEX7 gene structure, alternative transcripts, and evidence for a founder haplotype for the frequent RCDP allele, L292ter, GENOMICS, 63(2), 2000, pp. 181-192

Authors: Braverman, N Lin, P Moebius, FF Obie, C Moser, A Glossmann, H Wilcox, WR Rimoin, DL Smith, M Kratz, L Kelley, RI Valle, D
Citation: N. Braverman et al., Mutations in the gene encoding 3 beta-hydroxysteroid-Delta(8),Delta(7)-isomerase cause X-linked dominant Conradi-Hunermann syndrome, NAT GENET, 22(3), 1999, pp. 291-294
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