H. W. Moser

Adrenoleukodystrophy: evidence for X linkage, inactivation, and selection favoring the mutant allele in heterozygous cells.

Barbara R. Migeon, H. W. Moser, Ann B. Moser et al. · Proceedings of the National Academy of Sciences · 1981 · 290 citations · Full text

Mutant Allele, Metabolic Disorder, Genetics +17

Analysis of MRI patterns aids prediction of progression in X-linked adrenoleukodystrophy

Daniel J. Loes, Ali Fatemi, Elias R. Melhem et al. · Neurology · 2003 · 266 citations

The peroxisome biogenesis disorder group 4 gene, PXAAA1, encodes a cytoplasmic ATPase required for stability of the PTS1 receptor.

T. Yahraus, Nancy Braverman, Gabriele Dodt et al. · The EMBO Journal · 1996 · 187 citations · Full text

Signal Transduction, Molecular Research, Molecular Pathway +8

MR findings in adult-onset adrenoleukodystrophy.

Ashok Kumar, Wolfgang Köhler, B. Kruse et al. · PubMed · 1995 · 133 citations · Full text

Altered expression of ALDP in X-linked adrenoleukodystrophy.

Paul A. Watkins, Stephen J. Gould, Marilyn A. Smith et al. · PubMed · 1995 · 129 citations