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Juvenile-onset neuronal ceroid lipofuscinosis (CLN1) disease with a novel deletion and duplication in the PPT1 gene.

作者信息

Ozono Tatsuhiko, Kinoshita Makoto, Narita Aya, Hirakiyama Asami, Kosuga Motomichi, Okuyama Torayuki, Fukada Kei

机构信息

Department of Neurology, Osaka General Medical Center, 3-1-56, Mandai-higashi, Sumiyosh-ku, Osaka 558-8558, Japan.

Department of Child Neurology, Faculty of Medicine, Tottori University, 36-1 Nishi-cho, Yonago city, Tottori 683-8504, Japan.

出版信息

J Neurol Sci. 2018 May 15;388:4-6. doi: 10.1016/j.jns.2018.02.030. Epub 2018 Feb 21.

DOI:10.1016/j.jns.2018.02.030
PMID:29627028
Abstract
摘要

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A novel c.776_777insA mutation in CLN1 leads to infantile neuronal ceroid lipofuscinosis.CLN1基因中一种新的c.776_777insA突变导致婴儿神经元蜡样脂褐质沉积症。
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