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Mitochondrial GTPase mitofusin 2 mutation in Charcot–Marie–Tooth neuropathy type 2A

✍ Scribed by Kazuki Kijima; Chikahiko Numakura; Hiroko Izumino; Kazuo Umetsu; Atsuo Nezu; Toshihide Shiiki; Masafumi Ogawa; Yoshito Ishizaki; Takeshi Kitamura; Yasunobu Shozawa; Kiyoshi Hayasaka


Publisher
Springer
Year
2004
Tongue
English
Weight
222 KB
Volume
116
Category
Article
ISSN
0340-6717

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## BACKGROUND. A general predisposition for vincristine-related neuropathy has been observed in persons with a family history of hereditary neuropathies. ## METHODS. In a retrospective case series, we investigated the possible association between the DNA rearrangement found in patients with Cha