Biochemical and genetic characterization of an unusual mild PEX3- related Zellweger spectrum disorder-Reference-Cited by-同舟云学术

Biochemical and genetic characterization of an unusual mild PEX3- related Zellweger spectrum disorder

Published:2017-08 Issue:4 Volume:121 Page:325-328
ISSN:1096-7192
Container-title:Molecular Genetics and Metabolism
language:en
Short-container-title:Molecular Genetics and Metabolism

Author:

Bjørgo Kathrine,Fjær Roar,Mørk Hanne Håberg,Ferdinandusse Sacha,Falkenberg Kim D.,Waterham Hans R.,Øye Ane-Marte,Sikiric Alma,Amundsen Silja Svanstrøm,Kulseth Mari Ann,Selmer Kaja

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference13 articles.

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3. The role of conserved PEX3 regions in PEX19-binding and peroxisome biogenesis Traffic;Schmidt,2012

4. Peroxisome biogenesis disorders: biological, clinical and pathophysiological perspectives;Braverman;Dev. Disabil. Res. Rev.,2013

5. Peroxisome biogenesis disorders in the Zellweger spectrum: an overview of current diagnosis, clinical manifestations, and treatment guidelines;Braverman;Mol. Genet. Metab.,2016

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