Axonal Charcot-Marie-Tooth disease due to COQ7 mutation: expanding the genetic and clinical spectrum

Author:

Zhang Xin-Yun123,Dong Hai-Lin123,Wu Zhi-Ying1234ORCID

Affiliation:

1. Department of Medical Genetics and Center for Rare Diseases, Second Affiliated Hospital, Zhejiang University School of Medicine , Hangzhou 310009 , China

2. Liangzhu Laboratory, Zhejiang University Medical Center , Hangzhou 311121 , China

3. Department of Neurology in Second Affiliated Hospital, and Key Laboratory of Medical Neurobiology of Zhejiang Province, Zhejiang University School of Medicine , Hangzhou 310009 , China

4. NHC and CAMS Key Laboratory of Medical Neurobiology, MOE Frontier Science Center for Brain Science and Brain-machine Integration, School of Brain Science and Brain Medicine, Zhejiang University , Hangzhou 310012 , China

Funder

research foundation

Zhejiang University

Fundamental Research Funds

Central Universities

Publisher

Oxford University Press (OUP)

Subject

Neurology (clinical)

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