Heterozygous individuals with mild phenotype in late-onset glycogen storage disease type 2: a new cohort of patients?

BMC Musculoskeletal Disorders

Poster Presentation

关键词: Myopathy;    Enzyme Replacement Therapy;    Neuromuscular Disease;    Glycogen Storage Disease;    Pompe Disease;   

DOI  :  10.1186/1471-2474-14-S2-P12

来源: Springer

【 授权许可】

CC BY   
© Vercelli et al; licensee BioMed Central Ltd. 2013