Journal: Genes

Filtra

Data

Small Complex Rearrangement in HINT1-Related Axonal Neuropathy

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.

Torna in alto