Associated Papers
A rare case of pediatric recurrent rhabdomyolysis with compound heterogenous variants in the LPIN1.
Che R et al.
Bmc Pediatrics, 2020
Molecular analysis of LPIN1 in Jordanian patients with rhabdomyolysis.
Jaradat SA et al.
Meta Gene, 2016
Study of LPIN1, LPIN2 and LPIN3 in rhabdomyolysis and exercise-induced myalgia.
Michot C et al.
Journal of Inherited Metabolic Disease, 2012
LPIN1 gene mutations: a major cause of severe rhabdomyolysis in early childhood.
Michot C et al.
Human Mutation, 2010
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