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Clinical and molecular characterization of three patients with Hepatocerebral form of mitochondrial DNA depletion syndrome: a case series.
Mahjoub, Ghazale; Habibzadeh, Parham; Dastsooz, Hassan; Mirzaei, Malihe; Kavosi, Arghavan; Jamali, Laila; Javanmardi, Haniyeh; Katibeh, Pegah; Faghihi, Mohammad Ali; Dastgheib, Seyed Alireza.
Afiliación
  • Mahjoub G; Persian BayanGene Research and Training Center, Shiraz University of Medical Sciences, Shiraz, Iran.
  • Habibzadeh P; Persian BayanGene Research and Training Center, Shiraz University of Medical Sciences, Shiraz, Iran.
  • Dastsooz H; Student Research Committee, Shiraz University of Medical Sciences, Shiraz, Iran.
  • Mirzaei M; Persian BayanGene Research and Training Center, Shiraz University of Medical Sciences, Shiraz, Iran.
  • Kavosi A; Italian Institute for Genomic Medicine (IIGM), University of Turin, Turin, Italy.
  • Jamali L; Persian BayanGene Research and Training Center, Shiraz University of Medical Sciences, Shiraz, Iran.
  • Javanmardi H; Persian BayanGene Research and Training Center, Shiraz University of Medical Sciences, Shiraz, Iran.
  • Katibeh P; Persian BayanGene Research and Training Center, Shiraz University of Medical Sciences, Shiraz, Iran.
  • Faghihi MA; Student Research Committee, Shiraz University of Medical Sciences, Shiraz, Iran.
  • Dastgheib SA; Department of Pediatrics, Shiraz University of Medical Sciences, Shiraz, Iran.
BMC Med Genet ; 20(1): 167, 2019 10 29.
Article en En | MEDLINE | ID: mdl-31664948
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: ADN Mitocondrial / Enfermedades Mitocondriales Límite: Female / Humans / Infant / Male Idioma: En Revista: BMC Med Genet Asunto de la revista: GENETICA MEDICA Año: 2019 Tipo del documento: Article País de afiliación: Irán
Texto completo
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: ADN Mitocondrial / Enfermedades Mitocondriales Límite: Female / Humans / Infant / Male Idioma: En Revista: BMC Med Genet Asunto de la revista: GENETICA MEDICA Año: 2019 Tipo del documento: Article País de afiliación: Irán