CLC-3 deficiency leads to phenotypes similar to human neuronal ceroid lipofuscinosis-Reference-Cited by-同舟云学术

CLC-3 deficiency leads to phenotypes similar to human neuronal ceroid lipofuscinosis

Published:2002-06 Issue:6 Volume:7 Page:597-605
ISSN:1356-9597
Container-title:Genes to Cells
language:en
Short-container-title:

Author:

Yoshikawa Momono,Uchida Shinichi,Ezaki Junji,Rai Tatemitsu,Hayama Atsushi,Kobayashi Katsuki,Kida Yujiro,Noda Masaki,Koike Masato,Uchiyama Yasuo,Marumo Fumiaki,Kominami Eiki,Sasaki Sei

Publisher

Wiley

Subject

Cell Biology,Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1365-2443.2002.00539.x/fullpdf

Reference33 articles.

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3. A lysosomal proteinase, the late infantile neuronal ceroid lipofuscinosis gene (CLN2) product, is essential for degradation of a hydrophobic protein, the subunit c of ATP synthase;Ezaki;J. Neurochem.,1999

4. Pore forming segments in voltage-gated chloride channels;Fahlke;Nature,1997

5. The neuronal ceroid-lipofuscinoses;Goebel;J. Child. Neurol.,1995

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