Autori: Marinella G

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Natural history of Becker muscular dystrophy: DMD gene mutations predict clinical severity

KLHL40-Related Myopathy: A Systematic Review and Insight into a Follow-up Biomarker via a New Case Report.

Congenital Myopathy as a Phenotypic Expression of CACNA1S Gene Mutation: Case Report and Systematic Review of the Literature.

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