Acute recurrent rhabdomyolysis in a Chinese boy associated with a novel compound heterozygous LPIN1 variant: a case report
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DOI: 10.1186/s12883-021-02050-w
Abstract: Background LPIN1 -related acute recurrent rhabdomyolysis (RM), first reported in 2008, is an autosomal recessive inherited metabolic disease. In recent years, LPIN1 gene variants have been identified as one of the main causes of severe… read more here.
Keywords: acute recurrent; case; recurrent rhabdomyolysis; compound heterozygous ... See more keywords