The Pex1-G844D mouse: A model for mild human Zellweger spectrum disorder-Reference-Cited by-同舟云学术

The Pex1-G844D mouse: A model for mild human Zellweger spectrum disorder

Published:2014-04 Issue:4 Volume:111 Page:522-532
ISSN:1096-7192
Container-title:Molecular Genetics and Metabolism
language:en
Short-container-title:Molecular Genetics and Metabolism

Author:

Hiebler Shandi,Masuda Tomohiro,Hacia Joseph G.,Moser Ann B.,Faust Phyllis L.,Liu Anita,Chowdhury Nivedita,Huang Ning,Lauer Amanda,Bennett Jean,Watkins Paul A.,Zack Donald J.,Braverman Nancy E.,Raymond Gerald V.,Steinberg Steven J.

Funder

National Institutes of Health

Foundation Fighting Blindness

Research to Prevent Blindness

Guerrieri Family Foundation

Publisher

Elsevier BV

Subject

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

Reference62 articles.

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5. A novel defect of peroxisome division due to a homozygous non-sense mutation in the PEX11beta gene;Ebberink;J. Med. Genet.,2012

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