A nonsense mutation in the LIMP-2 gene associated with progressive myoclonic epilepsy and nephrotic syndrome-Reference-Cited by-同舟云学术

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A nonsense mutation in the LIMP-2 gene associated with progressive myoclonic epilepsy and nephrotic syndrome

Published:2008-04-15 Issue:14 Volume:17 Page:2238-2243
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:Human Molecular Genetics

Author:

Balreira A.,Gaspar P.,Caiola D.,Chaves J.,Beirao I.,Lima J. L.,Azevedo J. E.,Miranda M. C. S.

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/17/14/2238/2745771/ddn124.pdf

Reference31 articles.

1. The CD36, CLA-1 (CD36L1), and LIMPII (CD36L2) gene family: cellular distribution, chromosomal location, and genetic evolution

2. Isolation and sequencing of a cDNA clone encoding the 85 kDa human lysosomal sialoglycoprotein (hLGP85) in human metastatic pancreas islet tumor cells

3. Lysosomal membrane glycoproteins. Structure, biosynthesis, and intracellular trafficking.

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