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博士論文

COX10両アレル変異とPMP22欠失を伴ったLeigh脳症の一家系 : 臨床病理学的特徴と分子遺伝学的解析の検討

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COX10両アレル変異とPMP22欠失を伴ったLeigh脳症の一家系 : 臨床病理学的特徴と分子遺伝学的解析の検討

Persistent ID (NDL)
info:ndljp/pid/12263756
Material type
博士論文
Author
黒羽, 泰子
Publisher
-
Publication date
2021-03-23
Material Format
Digital
Capacity, size, etc.
-
Name of awarding university/degree
新潟大学,博士(医学)
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Notes on use

Note (General):

新大院博(医)第974号

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Digital

Material Type
博士論文
Author/Editor
黒羽, 泰子
Author Heading
Publication Date
2021-03-23
Publication Date (W3CDTF)
2021-03-23
Alternative Title
Clinicopathological and molecular features of a family with Leigh encephalopathy and hereditary neuropathy with liability to pressure palsy due to biallelic COX10 mutations and PMP22 deletion
Degree grantor/type
新潟大学
Date Granted
2021-03-23
Date Granted (W3CDTF)
2021-03-23