검색결과 : 2건
| No. | Article |
|---|---|
| 1 |
X-linked adrenoleukodystrophy phenotype is independent of ABCD2 genotype Maier EM, Mayerhofer PU, Asheuer M, Kohler W, Rothe M, Muntau AC, Roscher AA, Holzinger A, Aubourg P, Berger J Biochemical and Biophysical Research Communications, 377(1), 176, 2008 |
| 2 |
Molecular mechanism of detectable catalase-containing particles, peroxisomes, in fibroblasts from a PEX2-defective patient Shimozawa N, Zhang ZY, Imamura A, Suzuki Y, Fujiki Y, Tsukamoto T, Osumi T, Aubourg P, Wanders RJA, Kondo N Biochemical and Biophysical Research Communications, 268(1), 31, 2000 |