Peroxisomal acyl CoA oxidase deficiency

Author:

Suzuki Yasuyuki,Iai Mizue,Kamei Atsushi,Tanabe Yuzo,Chida Shoichi,Yamaguchi Seiji,Zhang Zhongyi,Takemoto Yasuhiko,Shimozawa Nobuyuki,Kondo Naomi

Publisher

Elsevier BV

Subject

Pediatrics, Perinatology and Child Health

Reference12 articles.

1. A new peroxisomal disorder with enlarged peroxisomes and a specific deficiency of acyl-CoA oxidase (pseudo- neonatal adrenoleukodystrophy);Poll-The;Am J Hum Genet,1988

2. Distinction between peroxisomal bifunctional enzyme and acyl-CoA oxidase deficiencies;Watkins;Ann Neurol,1995

3. First prenatal diagnosis of acyl-CoA oxidase deficiency;Wanders;J Inherit Metab Dis,1990

4. Novel subtype of peroxisomal acyl-CoA oxidase deficiency and bifunctional enzyme deficiency with detectable enzyme protein: identification by means of complementation analysis;Suzuki;Am J Hum Genet,1994

5. Incidence of peroxisomal disorders in Japan;Suzuki;Jpn J Hum Genet,1996

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