Identification of eight novel mutations of the acid alpha-glucosidase gene causing the infantile or juvenile form of glycogen storage disease type II. | J Neurol;255(6): 831-8, 2008 Jun. | MEDLINE

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Identification of eight novel mutations of the acid alpha-glucosidase gene causing the infantile or juvenile form of glycogen storage disease type II.

Wan, L; Lee, C-C; Hsu, C-M; Hwu, W-L; Yang, C-C; Tsai, C-H; Tsai, F-J.

Affiliation

Wan L; Dept. of Medical Genetics and Medical, Research, China Medical University Hospital, No. 2 Yuh-Der Road, Taichung, Taiwan.

J Neurol ; 255(6): 831-8, 2008 Jun.

Article in En | MEDLINE | ID: mdl-18458862

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Glycogen Storage Disease Type II / Genetic Predisposition to Disease / Alpha-Glucosidases / Mutation Type of study: Diagnostic_studies Limits: Adult / Humans / Middle aged Country/Region as subject: Asia Language: En Journal: J Neurol Year: 2008 Document type: Article Affiliation country: Country of publication:

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Glycogen Storage Disease Type II / Genetic Predisposition to Disease / Alpha-Glucosidases / Mutation Type of study: Diagnostic_studies Limits: Adult / Humans / Middle aged Country/Region as subject: Asia Language: En Journal: J Neurol Year: 2008 Document type: Article Affiliation country: Country of publication: