Identification of Novel ARSA Mutations in Chinese Patients with Metachromatic Leukodystrophy

Identification of Novel ARSA Mutations in Chinese Patients with Metachromatic Leukodystrophy

Objective. Metachromatic leukodystrophy (MLD) is an inherited disease caused by a deficiency of the enzyme arylsulfatase A (ARSA) that leads to severe physiologic and developmental problems. Our study is aimed at elucidating the clinical and genetic characteristics of Chinese MLD patients. Methods....

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Main Authors: Li Chen, Huifang Yan, Binbin Cao, Ye Wu, Qiang Gu, Jiangxi Xiao, Yanling Yang, Huixia Yang, Zhen Shi, Zhixian Yang, Hong Pan, Xingzhi Chang, Junya Chen, Yu Sun, Yuehua Zhang, Xiru Wu, Yuwu Jiang, Jingmin Wang
Format: Article
Language:English
Published: Wiley 2018-01-01
Series:International Journal of Genomics
Online Access:http://dx.doi.org/10.1155/2018/2361068
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http://dx.doi.org/10.1155/2018/2361068

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