(Q41717979)

7 October 2017

Peroxisomal disorders: complementation analysis using beta-oxidation of very long chain fatty acids (English)

1 reference

7 October 2017

0 references

McGuinness MC

1

1 reference

7 October 2017

Moser AB

series ordinal

2

1 reference

7 October 2017

Moser HW

series ordinal

3

1 reference

7 October 2017

Watkins PA

series ordinal

4

1 reference

7 October 2017

1 October 1990

1 reference

Biochemical and Biophysical Research Communications

7 October 2017

1 reference

7 October 2017

172

1 reference

7 October 2017

1

1 reference

7 October 2017

364-369

1 reference

Peroxisomal disorders in neurology

7 October 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2805%2980218-9

Genetic and phenotypic heterogeneity in disorders of peroxisome biogenesis--a complementation study involving cell lines from 19 patients

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2805%2980218-9

Genetic heterogeneity in the cerebrohepatorenal (Zellweger) syndrome and other inherited disorders with a generalized impairment of peroxisomal functions. A study using complementation analysis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2805%2980218-9

In situ genetic complementation analysis of cells with generalized peroxisomal dysfunction

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2805%2980218-9

Phytanic acid alpha-oxidation and complementation analysis of classical Refsum and peroxisomal disorders

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2805%2980218-9

Peroxisomal bifunctional enzyme deficiency

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2805%2980218-9

Biochemical abnormalities in rhizomelic chondrodysplasia punctata

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2805%2980218-9

Neonatal seizures and retardation in a girl with biochemical features of X-linked adrenoleukodystrophy: a possible new peroxisomal disease entity

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2805%2980218-9

Translocation of acyl-CoA oxidase into peroxisomes requires ATP hydrolysis but not a membrane potential

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2805%2980218-9

10.1016/S0006-291X(05)80218-9

7 January 2021

Identifiers

DOI

1 reference

7 October 2017

1 reference