Case Report of RANBP2 Mutation and Familial Acute Necrotizing Encephalopathy.

Paktinat, Mohamad; Hessami, Kamran; Inaloo, Soroor; Nemati, Hamid; Katibeh, Pegah; Nejabat, Marzieh; Darabi, Mohammad Hassan; Bereshneh, Ali Hosseini

Paktinat, Mohamad; Hessami, Kamran; Inaloo, Soroor; Nemati, Hamid; Katibeh, Pegah; Nejabat, Marzieh; Darabi, Mohammad Hassan; Bereshneh, Ali Hosseini.

Afiliación

Paktinat M; Neonatology Research Center, Neuroscience Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.
Hessami K; Student Research Committee, Shiraz University of Medical Sciences, Shiraz, Iran.
Inaloo S; Maternal-Fetal Medicine Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.
Nemati H; Neonatology Research Center, Neuroscience Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.
Katibeh P; Neonatology Research Center, Neuroscience Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.
Nejabat M; Neonatology Research Center, Neuroscience Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.
Darabi MH; Neonatology Research Center, Neuroscience Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.
Bereshneh AH; Student Research Committee, Shiraz University of Medical Sciences, Shiraz, Iran.

Int J Pediatr ; 2021: 6695119, 2021.

Article en En | MEDLINE | ID: mdl-33777149

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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Tipo de estudio: Screening_studies Idioma: En Revista: Int J Pediatr Año: 2021 Tipo del documento: Article País de afiliación: Irán

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