The Turkish Journal of Pediatrics 2020 , Vol 62 , Num 4
A neglected cause of recurrent rhabdomyolysis, LPIN1 gene defect: a rare case from Turkey
Sevgi Topal 1 ,Melis Demir Köse 2 ,Hasan Ağın 1 ,Ferhat Sarı 3 ,Mustafa Çolak 1 ,Gülhan Atakul 1 ,Utku Karaarslan 1 ,Rana İşgüder 4
1 Departments of Pediatric Intensive Care Unit, Dr. Behcet Uz Children’s Diseases and Surgery Training and Research Hospital, İzmir
2 Pediatric Metabolism and Nutrition, Dr. Behcet Uz Children’s Diseases and Surgery Training and Research Hospital, İzmir
3 Department of Pediatric Intensive Care Unit, Şişli Hamidiye Etfal Training and Research Hospital, İstanbul, Turkey
4 Department of Child Health and Diseases, University of Health Sciences, Dr. Behcet Uz Children’s Diseases and Surgery Training and Research Hospital, İzmir
DOI : 10.24953/turkjped.2020.04.015 Keywords :
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