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Novel mutations of SAR1B gene in four children with chylomicron retention disease.
Simone, Maria Luisa; Rabacchi, Claudio; Kuloglu, Zarife; Kansu, Aydan; Ensari, Arzu; Demir, Arzu Meltem; Hizal, Gulin; Di Leo, Enza; Bertolini, Stefano; Calandra, Sebastiano; Tarugi, Patrizia.
Afiliación
  • Simone ML; Department of Life Sciences, University of Modena and Reggio Emilia, Modena, Italy.
  • Rabacchi C; Department of Life Sciences, University of Modena and Reggio Emilia, Modena, Italy.
  • Kuloglu Z; Department of Pediatric Gastroenterology, Hepatology and Nutrition, Ankara University, Ankara, Turkey.
  • Kansu A; Department of Pediatric Gastroenterology, Hepatology and Nutrition, Ankara University, Ankara, Turkey.
  • Ensari A; Department of Pediatric Gastroenterology, Hepatology and Nutrition, Ankara University, Ankara, Turkey.
  • Demir AM; University of Health Sciences, Ankara Child Health and Diseases Hematology Oncology Training and Research Hospital, Ankara, Turkey.
  • Hizal G; University of Health Sciences, Ankara Child Health and Diseases Hematology Oncology Training and Research Hospital, Ankara, Turkey.
  • Di Leo E; Department of Life Sciences, University of Modena and Reggio Emilia, Modena, Italy.
  • Bertolini S; Department of Internal Medicine, University of Genova, Genova, Italy.
  • Calandra S; Department of Biomedical, Metabolic and Neurological Sciences, University of Modena and Reggio Emilia, Modena, Italy.
  • Tarugi P; Department of Life Sciences, University of Modena and Reggio Emilia, Modena, Italy. Electronic address: tarugi@unimore.it.
J Clin Lipidol ; 13(4): 554-562, 2019.
Article en En | MEDLINE | ID: mdl-31253576

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Proteínas de Unión al GTP Monoméricas / Hipobetalipoproteinemias / Síndromes de Malabsorción Tipo de estudio: Prognostic_studies Límite: Child / Child, preschool / Humans / Infant / Male Idioma: En Revista: J Clin Lipidol Asunto de la revista: BIOQUIMICA / METABOLISMO Año: 2019 Tipo del documento: Article País de afiliación: Italia

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Proteínas de Unión al GTP Monoméricas / Hipobetalipoproteinemias / Síndromes de Malabsorción Tipo de estudio: Prognostic_studies Límite: Child / Child, preschool / Humans / Infant / Male Idioma: En Revista: J Clin Lipidol Asunto de la revista: BIOQUIMICA / METABOLISMO Año: 2019 Tipo del documento: Article País de afiliación: Italia