Mutation in the Scyl1 gene encoding amino‐terminal kinase‐like protein causes a recessive form of spinocerebellar neurodegeneration-Reference-Cited by-同舟云学术

Mutation in the Scyl1 gene encoding amino‐terminal kinase‐like protein causes a recessive form of spinocerebellar neurodegeneration

Published:2007-06-15 Issue:7 Volume:8 Page:691-697
ISSN:1469-221X
Container-title:EMBO reports
language:en
Short-container-title:EMBO Rep

Author:

Schmidt Wolfgang M¹²,Kraus Cornelia³,Höger Harald⁴,Hochmeister Sonja⁵,Oberndorfer Felicitas¹,Branka Manuela¹,Bingemann Sonja¹,Lassmann Hans⁵,Müller Markus²,Macedo‐Souza Lúcia Inês⁶,Vainzof Mariz⁶,Zatz Mayana⁶,Reis André³,Bittner Reginald E¹

Affiliation:

1. Neuromuscular Research Department, Center of Anatomy & Cell Biology, Medical University of Vienna Währinger Strasse 13 A‐1090 Vienna Austria

2. Department of Clinical Pharmacology, Section of Cardiovascular Medicine, Medical University of Vienna Währinger Gürtel 18‐20 A‐1090 Vienna Austria

3. Institute of Human Genetics, Friedrich‐Alexander‐University Erlangen‐Nuremberg Schwabachanlage 10 D‐91054 Erlangen Germany

4. Division for Laboratory Animal Science and Genetics, Medical University of Vienna Brauhausgasse 34 A‐2325 Himberg Austria

5. Center for Brain Research, Division of Neuroimmunology, Medical University of Vienna Spitalgasse 4 A‐1090 Vienna Austria

6. Department of Biology, Institute of Biological Sciences and Center for Study of Human Genome, University of São Paulo, Rua do Matão, 277 Cidade Universitária São Paulo Brazil

Publisher

EMBO

Subject

Genetics,Molecular Biology,Biochemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1038/sj.embor.7401001

Reference12 articles.

1. The Mouse Mutation Muscle Deficient (mdf) is Characterized by a Progressive Motoneuron Disease

2. The Ataxia-ome: Connecting Disease Proteins of the Cerebellum

3. Identification and Characterization of the Human Protein Kinase-like Gene NTKL: Mitosis-Specific Centrosomal Localization of an Alternatively Spliced Isoform

4. Genome-wide atlas of gene expression in the adult mouse brain

5. A Protein–Protein Interaction Network for Human Inherited Ataxias and Disorders of Purkinje Cell Degeneration

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