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博士論文

A novel point mutation (G[-1] to T) in a 5' splice donor site of intron 13 of the dystrophin gene results in exon skipping and is responsible for Becker muscular dystrophy

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A novel point mutation (G[-1] to T) in a 5' splice donor site of intron 13 of the dystrophin gene results in exon skipping and is responsible for Becker muscular dystrophy

Call No. (NDL)
UT51-95-V402
Bibliographic ID of National Diet Library
000000290165
Persistent ID (NDL)
info:ndljp/pid/3105545
Material type
博士論文
Author
萩原容子 [著]
Publisher
-
Date granted
平成7年7月12日
Material Format
Paper・Digital
Capacity, size, etc.
-
Degree grantor and degree
神戸大学,博士 (医学)
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博士論文

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Paper Digital

Material Type
博士論文
Title
A novel point mutation (G[-1] to T) in a 5' splice donor site of intron 13 of the dystrophin gene results in exon skipping and is responsible for Becker muscular dystrophy
Author/Editor
萩原容子 [著]
Author Heading
萩原, 容子 ハギワラ, ヨウコ
Alternative Title
Becker型筋ジストロフィー患者で発見されたエクソンのスキッピングを引き起こすジストロフィン遺伝子の新しい点突然変異 Becker ガタ キンジストロフィー カンジャ デ ハッケンサレタ エクソン ノ スキッピング オ ヒキオコス ジストロフィン イデンシ ノ アタラシイ テン トツゼン ヘンイ
Degree Grantor
神戸大学
Date Granted
平成7年7月12日
Date Granted (W3CDTF)
1995
Dissertation Number
乙第1945号
Degree Type
博士 (医学)