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Article

A novel CLN2/TPP1 mutation in a Chinese patient with late infantile neuronal ceroid lipofuscinosis.

Neurogenetics - 1 Feb 2011

Wang Yu-Liang, Zeng Zhi-Yong, Song Xing-Wang, Hao Zhuo-Fang, Shi Yi-Wu, Tang Bin, Chen Sheng-Qiang, Gao Mei-Mei, Di Wei, Long Yue-Sheng, Yi Yong-Hong, Liao Wei-Ping

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Identifiers

PMID: 20820830
DOI: 10.1007/s10048-010-0258-1

Genes

TPP1

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A novel CLN2/TPP1 mutation in a Chinese patient with late infantile neuronal ceroid lipofuscinosis.PMID 20820830Read ↗

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