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

EMBO Reports

Volumn 8, Issue 7, 2007, Pages 691-697

  Schmidt, Wolfgang M ^a   Kraus, Cornelia ^b   Höger, Harald ^a   Hochmeister, Sonja ^c   Oberndorfer, Felicitas ^a   Branka, Manuela ^a   Bingemann, Sonja ^a   Lassmann, Hans ^c   Müller, Markus ^a   Macedo Souza, Lúcia Inês ^d   Vainzof, Mariz ^d   Zatz, Mayana ^d   Reis, André ^b   Bittner, Reginald E ^a  

^a MEDICAL UNIVERSITY OF VIENNA   (Austria)

^b UNIVERSITY OF ERLANGEN NUREMBERG   (Germany)

^c Medical University of Vienna   (Austria)

^d UNIVERSITY OF SÃO PAULO   (Brazil)

Author keywords

[No Author keywords available]

Indexed keywords

NERVE PROTEIN; SACCHAROMYCES CEREVISIAE LIKE 1 PROTEIN; UNCLASSIFIED DRUG;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; CELL LOSS; CEREBELLUM ATROPHY; CONTROLLED STUDY; GENE MUTATION; GENETIC CODE; HISTOPATHOLOGY; HUMAN; HUMAN CELL; MOUSE; NEUROMUSCULAR SYNAPSE; NONHUMAN; NUCLEOTIDE SEQUENCE; OPTIC NERVE ATROPHY; PRIORITY JOURNAL; PROTEIN EXPRESSION; PURKINJE CELL; RECESSIVE GENE; RECESSIVE INHERITANCE; SPINOCEREBELLAR DEGENERATION;

ANIMALIA; MURINAE;

EID: 34447098034     PISSN: 1469221X     EISSN: 14693178     Source Type: Journal    
DOI: 10.1038/sj.embor.7401001     Document Type: Article

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