Biblio

Found 3 results

2008

Steinberg S, Jones R, Tiffany C, Moser A. 2008. Investigational methods for peroxisomal disorders.. Current protocols in human genetics / editorial board, Jonathan L. Haines ... [et al.]. Chapter 17:Unit17.6. Abstract

2005

Mahmood A, Dubey P, Moser HW, Moser A. 2005. X-linked adrenoleukodystrophy: therapeutic approaches to distinct phenotypes.. Pediatric transplantation. 9 Suppl 7:55-62. Abstract

2004

Steinberg S, Chen L, Wei L, Moser A, Moser H, Cutting G, Braverman N. 2004. The PEX Gene Screen: molecular diagnosis of peroxisome biogenesis disorders in the Zellweger syndrome spectrum.. Molecular genetics and metabolism. 83(3):252-63. Abstract