Clinical and genetic analysis of a case with centronuclear myopathy caused by SPEG gene mutation: a case report and literature review

Overview of attention for article published in BMC Pediatrics, April 2021

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SPEG

Cited by user Iztwoz on 06 Jun 2021

Striated muscle preferentially expressed protein kinase, in the human is encoded by the SPEG gene, a member of the myosin light chain kinase protein family.

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