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Harmonizing care for rare diseases: How we developed the mitochondrial care network in the United States.
Karaa, Amel; Goldstein, Amy; Balcells, Cristy; Mann, Kira; Stanley, Laura; Yeske, Philip E; Parikh, Sumit.
  • Karaa A; Department of Genetics, Massachusetts General Hospital, Boston, MA, United States of America. Electronic address: akaraa@mgh.harvard.edu.
  • Goldstein A; Human Genetics, Children's Hospital of Philadelphia, Philadelphia, PA, United States of America.
  • Balcells C; MitoAction, Boston, MA, United States of America.
  • Mann K; MitoAction, Boston, MA, United States of America.
  • Stanley L; Foundation for Mitochondrial Medicine, Atlanta, GA, United States of America.
  • Yeske PE; United Mitochondrial Disease Foundation, Pittsburgh, PA, United States of America.
  • Parikh S; Neurogenetics, Center for Pediatric Neurology, Cleveland Clinic Children's Hospital, Cleveland, OH, United States of America.
Mol Genet Metab ; 127(2): 122-127, 2019 06.
Article en En | MEDLINE | ID: mdl-31138493
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Enfermedades Mitocondriales / Enfermedades Raras / Servicios de Información Tipo de estudio: Diagnostic_studies / Guideline Límite: Humans País como asunto: America do norte Idioma: En Año: 2019 Tipo del documento: Article
Texto completo
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PubMed Links
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Enfermedades Mitocondriales / Enfermedades Raras / Servicios de Información Tipo de estudio: Diagnostic_studies / Guideline Límite: Humans País como asunto: America do norte Idioma: En Año: 2019 Tipo del documento: Article