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Concomitant MPZ and MFN2 Gene Variants and Charcot Marie Tooth Disease in a Boy: Clinical and Genetic Analysis-Literature Review.
Comella, M; Collotta, A; Pavone, V; Ciccia, L; Bellinvia, A; Cerruto, C; Biondi, M G L; Pisani, F; Pavone, P.
Afiliação
  • Comella M; Postgraduate Training Program in Pediatrics, Department of Clinical and Experimental Medicine, University of Catania, Catania 95123, Italy.
  • Collotta A; Postgraduate Training Program in Pediatrics, Department of Clinical and Experimental Medicine, University of Catania, Catania 95123, Italy.
  • Pavone V; Department of General Surgery and Medical Surgical Specialties, Section of Orthopaedics and Traumatology, University Hospital Policlinico "Rodolico-San Marco", University of Catania, Catania 95123, Italy.
  • Ciccia L; Postgraduate Training Program in Pediatrics, Department of Clinical and Experimental Medicine, University of Catania, Catania 95123, Italy.
  • Bellinvia A; Postgraduate Training Program in Pediatrics, Department of Clinical and Experimental Medicine, University of Catania, Catania 95123, Italy.
  • Cerruto C; Postgraduate Training Program in Pediatrics, Department of Clinical and Experimental Medicine, University of Catania, Catania 95123, Italy.
  • Biondi MGL; Postgraduate Training Program in Pediatrics, Department of Clinical and Experimental Medicine, University of Catania, Catania 95123, Italy.
  • Pisani F; Child Neuropsychiatric Unit, University Hospital of Parma, Italy-Medicine & Surgery Department, Via Gramsci, 14, Parma 43126, Italy.
  • Pavone P; Unit of Clinical Pediatrics, AOU "Policlinico", PO "G.Rodolico", University of Catania, Catania, Italy.
Case Rep Pediatr ; 2022: 3793226, 2022.
Article em En | MEDLINE | ID: mdl-35449525

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article