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A family with hereditary cerebellar ataxia finally confirmed as Gerstmann-Sträussler-Scheinker syndrome with P102L mutation in PRNP gene
Ling Long, Xiaodong Cai, Yaqing Shu and Zhengqi Lu
Neurosciences Journal April 2017, 22 (2) 138-142; DOI: https://doi.org/10.17712/nsj.2017.2.20160522
Ling Long
From the Department of Neurology (Long, Shu, Lu), The Third Affiliated Hospital of Sun Yat-Sen University, and from the Department of Neurology (Cai), The Sixth Affiliated Hospital of Sun Yat-Sen University, Guangzhou 510655, Guangdong, People’s Republic of China
MD, PhDXiaodong Cai
From the Department of Neurology (Long, Shu, Lu), The Third Affiliated Hospital of Sun Yat-Sen University, and from the Department of Neurology (Cai), The Sixth Affiliated Hospital of Sun Yat-Sen University, Guangzhou 510655, Guangdong, People’s Republic of China
MD, PhDYaqing Shu
From the Department of Neurology (Long, Shu, Lu), The Third Affiliated Hospital of Sun Yat-Sen University, and from the Department of Neurology (Cai), The Sixth Affiliated Hospital of Sun Yat-Sen University, Guangzhou 510655, Guangdong, People’s Republic of China
MscZhengqi Lu
From the Department of Neurology (Long, Shu, Lu), The Third Affiliated Hospital of Sun Yat-Sen University, and from the Department of Neurology (Cai), The Sixth Affiliated Hospital of Sun Yat-Sen University, Guangzhou 510655, Guangdong, People’s Republic of China
MD, PhD
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A family with hereditary cerebellar ataxia finally confirmed as Gerstmann-Sträussler-Scheinker syndrome with P102L mutation in PRNP gene
Ling Long, Xiaodong Cai, Yaqing Shu, Zhengqi Lu
Neurosciences Journal Apr 2017, 22 (2) 138-142; DOI: 10.17712/nsj.2017.2.20160522
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