Phenotype of patients with peroxisomal disorders subdivided into sixteen complementation groups (Q71700951)

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20 October 2019

title

Phenotype of patients with peroxisomal disorders subdivided into sixteen complementation groups (English)

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20 October 2019

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A B Moser

1

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20 October 2019

M Rasmussen

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20 October 2019

S Naidu

3

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20 October 2019

P A Watkins

4

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20 October 2019

M McGuinness

5

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20 October 2019

A K Hajra

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20 October 2019

G Chen

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G Raymond

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A Liu

9

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20 October 2019

D Gordon

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language of work or name

English

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publication date

1 July 1995

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The Journal of Pediatrics

20 October 2019

published in

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20 October 2019

volume

127

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20 October 2019

issue

1

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20 October 2019

page(s)

13-22

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Protein import into peroxisomes and biogenesis of the organelle

20 October 2019

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Mutations in the PTS1 receptor gene, PXR1, define complementation group 2 of the peroxisome biogenesis disorders

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Human alkyldihydroxyacetonephosphate synthase deficiency: a new peroxisomal disorder

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Biochemical abnormalities in rhizomelic chondrodysplasia punctata

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Pseudo-Zellweger syndrome: deficiencies in several peroxisomal oxidative activities

7 January 2021

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Cytosolic compartmentalization of hepatic alanine:glyoxylate aminotransferase in patients with aberrant peroxisomal biogenesis and its effect on oxalate metabolism

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7 January 2021

Identifiers

DOI

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20 October 2019

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