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المؤلفون: Hironao Saegusa, Yasuko Komatsuzaki, Kiyoshi Ohwada, Ichiro Kanazawa, Shin'ichi Shoji, Masahiko Watanabe, Hiroyuki Iwamoto, Tsuneo Fujita, Norio Ohkoshi, Hideyuki Toriyama, K. Ishikawa, HidehiroMizusawa, Hiroto Fujigasaki, Tsutomu Tanabe, Shuta Toru
المصدر: Human Molecular Genetics. 8:1185-1193
مصطلحات موضوعية: Cytoplasm, congenital, hereditary, and neonatal diseases and abnormalities, Cerebellum, Purkinje cell, Apoptosis, Biology, PC12 Cells, Purkinje Cells, Autosomal dominant cerebellar ataxia, Genetics, medicine, Animals, Humans, Spinocerebellar ataxia type 6, RNA, Messenger, Molecular Biology, Cells, Cultured, Genetics (clinical), Spinocerebellar Degenerations, Calcium channel, Neurodegeneration, Brain, General Medicine, Polyglutamine tract, medicine.disease, Rats, Cell biology, medicine.anatomical_structure, Calcium Channels, Peptides, Trinucleotide Repeat Expansion, Trinucleotide repeat expansion
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fda5ff3e699377bc37a867552bfb5d1a
https://doi.org/10.1093/hmg/8.7.1185