GAA compound heterozygous mutations associated with autophagic impairment cause cerebral infarction in Pompe disease | Aging
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Novel GAA Variants and Mosaicism in Pompe Disease Identified by Extended Analyses of Patients with an Incomplete DNA Diagnosis: Molecular Therapy - Methods & Clinical Development
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GAA compound heterozygous mutations associated with autophagic impairment cause cerebral infarction in Pompe disease | Aging
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