A Hereditary Spastic Paraplegia Mouse Model Supports a Role of ZFYVE26/SPASTIZIN for the Endolysosomal System-Reference-Cited by-同舟云学术

A Hereditary Spastic Paraplegia Mouse Model Supports a Role of ZFYVE26/SPASTIZIN for the Endolysosomal System

Published:2013-12-19 Issue:12 Volume:9 Page:e1003988
ISSN:1553-7404
Container-title:PLoS Genetics
language:en
Short-container-title:PLoS Genet

Author:

Khundadze Mukhran,Kollmann Katrin,Koch Nicole,Biskup Christoph,Nietzsche Sandor,Zimmer Geraldine,Hennings J. Christopher,Huebner Antje K.,Symmank Judit,Jahic Amir,Ilina Elena I.,Karle Kathrin,Schöls Ludger,Kessels Michael,Braulke Thomas,Qualmann Britta,Kurth Ingo,Beetz Christian,Hübner Christian A.

Publisher

Public Library of Science (PLoS)

Subject

Cancer Research,Genetics(clinical),Genetics,Molecular Biology,Ecology, Evolution, Behavior and Systematics

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5. Identification of the SPG15 gene, encoding spastizin, as a frequent cause of complicated autosomal-recessive spastic paraplegia, including Kjellin syndrome;S Hanein;Am J Hum Genet,2008

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