A Pex7 hypomorphic mouse model for plasmalogen deficiency affecting the lens and skeleton-Reference-Cited by-同舟云学术

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A Pex7 hypomorphic mouse model for plasmalogen deficiency affecting the lens and skeleton

Published:2010-04 Issue:4 Volume:99 Page:408-416
ISSN:1096-7192
Container-title:Molecular Genetics and Metabolism
language:en
Short-container-title:Molecular Genetics and Metabolism

Author:

Braverman Nancy,Zhang Rui,Chen Li,Nimmo Graeme,Scheper Sarah,Tran Tammy,Chaudhury Rupsa,Moser Ann,Steinberg Steven

Publisher

Elsevier BV

Subject

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

Reference53 articles.

1. Natural history of rhizomelic chondrodysplasia punctata;White;Am. J. Med. Genet.,2003

2. Peroxisome biogenesis disorders;Steinberg;Biochim. Biophys. Acta,2006

3. Cerebellar atrophy in chronic rhizomelic chondrodysplasia punctata: a potential role for phytanic acid and calcium in the death of its Purkinje cells;Powers;Acta Neuropathol. (Berl.),1999

4. MRI of the brain and cervical spinal cord in rhizomelic chondrodysplasia punctata;Bams-Mengerink;Neurology,2006

5. Human PEX7 encodes the peroxisomal PTS2 receptor and is responsible for rhizomelic chondrodysplasia punctata;Braverman;Nat. Genet.,1997

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