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Extension of the phenotypic spectrum of GLE1 ‐related disorders to a mild congenital form resembling congenital myopathy

Mathieu Cerino et al.
HAL (France) · Papers · License: Open Access
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mutationmyopathyngs
GLE1, Myopathy, Congenital, Mild, Mutation, NGS, 1, 0
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Record · ID 1066351
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