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    A neglected cause of recurrent rhabdomyolysis, LPIN1 gene defect: a rare case from Turkey

    A neglected cause of recurrent rhabdomyolysis, LPIN1 gene defect: a rare case from Turkey by Sevgi Topal, Melis Demir Köse, Hasan Ağın, Ferhat Sarı, Mustafa Çolak, Gülhan Atakul, Utku Karaarslan, Rana İşgüder

    Published 2020-08-01
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