Results 241 to 249 of about 1,353,029 (249)

Identification of novel mutations and sequence variation in the Zellweger syndrome spectrum of peroxisome biogenesis disorders

Human Mutation, 2009
Ann Moser
exaly  

Human Genome and Diseases:¶Cellular and molecular aspects of Zellweger syndrome and other peroxisome biogenesis disorders

Cellular and Molecular Life Sciences, 2002
Jutta Gärtner
exaly  

Genetic heterogeneity of peroxisome biogenesis disorders among Japanese patients: Evidence for a founder haplotype for the most commonPEX10 gene mutation

American Journal of Medical Genetics Part A, 2003
Nobuyuki Shimozawa
exaly  

Peroxisome biogenesis and the role of protein import

Journal of Cellular and Molecular Medicine, 2003
Alison Baker
exaly  

[Biogenesis of peroxisomes and human peroxisomal disorders].

Seikagaku. The Journal of Japanese Biochemical Society, 1995
openaire   +1 more source

[Peroxisome biogenesis and human disorders].

Tanpakushitsu kakusan koso. Protein, nucleic acid, enzyme, 2000
Y, Fujiki, K, Okumoto
openaire   +1 more source

Approaches to Studies on Peroxisome Biogenesis and Human Peroxisome‐deficient Disorders

Annals of the New York Academy of Sciences, 1996
openaire   +2 more sources

[Peroxisome biogenesis and human disorders].

Seikagaku. The Journal of Japanese Biochemical Society, 2003
openaire   +1 more source

TREATMENT OF PEROXISOME BIOGENESIS DISORDER

2015
openaire   +1 more source