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Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
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A novel SLC20A2 gene mutation causing primary familial brain calcification in an Ukrainian patient
Mariano Oliva1, Guglielmo Capaldo1, Alessandra D'Amico2
1Dipartimento di Scienze Mediche Chirurgiche Neurologiche Metaboliche e dell'Invecchiamento, Università degli studi della Campania Luigi Vanvitelli, P.zza Miraglia 2, 80138, Naples, Italy.
Abstract
No abstract available in PubMed .
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