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