A novel mutation in the C2 domain of protein kinase C gamma associated with spinocerebellar ataxia type 14. [electronic resource]

By:

Ueda, Takehiro

Contributor(s):

Seki, Tsuneyoshi
Katanazaka, Kimitaka
Sekiguchi, Kenji
Kobayashi, Kazuhiro
Kanda, Fumio
Toda, Tatsushi

Producer: 20140115Description: 1664-6 p. digitalISSN:

1432-1459

Subject(s):

Amino Acid Sequence
Base Sequence
Brain -- pathology
Female
Humans
Male
Middle Aged
Molecular Sequence Data
Mutation
Pedigree
Polymerase Chain Reaction
Protein Kinase C -- genetics
Spinocerebellar Ataxias
Spinocerebellar Degenerations -- genetics

Online resources:

Available from publisher's website

In: Journal of neurology vol. 260

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A novel mutation in the C2 domain of protein kinase C gamma associated with spinocerebellar ataxia type 14.

APA

Ueda T., Seki T., Katanazaka K., Sekiguchi K., Kobayashi K., Kanda F. & Toda T. (20140115). A novel mutation in the C2 domain of protein kinase C gamma associated with spinocerebellar ataxia type 14. : Journal of neurology.

Chicago

Ueda Takehiro, Seki Tsuneyoshi, Katanazaka Kimitaka, Sekiguchi Kenji, Kobayashi Kazuhiro, Kanda Fumio and Toda Tatsushi. 20140115. A novel mutation in the C2 domain of protein kinase C gamma associated with spinocerebellar ataxia type 14. : Journal of neurology.

Harvard

Ueda T., Seki T., Katanazaka K., Sekiguchi K., Kobayashi K., Kanda F. and Toda T. (20140115). A novel mutation in the C2 domain of protein kinase C gamma associated with spinocerebellar ataxia type 14. : Journal of neurology.

MLA

Ueda Takehiro, Seki Tsuneyoshi, Katanazaka Kimitaka, Sekiguchi Kenji, Kobayashi Kazuhiro, Kanda Fumio and Toda Tatsushi. A novel mutation in the C2 domain of protein kinase C gamma associated with spinocerebellar ataxia type 14. : Journal of neurology. 20140115.

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