A novel CLN2/TPP1 mutation in a Chinese patient with late infantile neuronal ceroid lipofuscinosis.
Wang YL, Zeng ZY, Song XW, Hao ZF, Shi YW, Tang B, Chen SQ, Gao MM, Di W, Long YS, Yi YH, Liao WP.
Wang YL, et al. Among authors: long ys.
Neurogenetics. 2011 Feb;12(1):93-5. doi: 10.1007/s10048-010-0258-1. Epub 2010 Sep 7.
Neurogenetics. 2011.
PMID: 20820830
No abstract available.