Your browser doesn't support javascript.
loading
Generation of a human iPSC line, FINCBi001-A, carrying a homoplasmic m.G3460A mutation in MT-ND1 associated with Leber's Hereditary optic Neuropathy (LHON).
Peron, Camille; Mauceri, Roberta; Cabassi, Tommaso; Segnali, Alice; Maresca, Alessandra; Iannielli, Angelo; Rizzo, Ambra; Sciacca, Francesca L; Broccoli, Vania; Carelli, Valerio; Tiranti, Valeria.
Afiliação
  • Peron C; Unit of Medical Genetics and Neurogenetics, Fondazione IRCCS Istituto Neurologico "Carlo Besta", Milan, Italy.
  • Mauceri R; Unit of Medical Genetics and Neurogenetics, Fondazione IRCCS Istituto Neurologico "Carlo Besta", Milan, Italy.
  • Cabassi T; Unit of Medical Genetics and Neurogenetics, Fondazione IRCCS Istituto Neurologico "Carlo Besta", Milan, Italy.
  • Segnali A; Unit of Medical Genetics and Neurogenetics, Fondazione IRCCS Istituto Neurologico "Carlo Besta", Milan, Italy.
  • Maresca A; IRCCS Istituto delle Scienze Neurologiche di Bologna, Bologna, Italy.
  • Iannielli A; Division of Neuroscience, San Raffaele Scientific Institute, Milan, Italy; National Research Council (CNR), Institute of Neuroscience, Milan, Italy.
  • Rizzo A; Laboratory of Clinical Investigation, Fondazione IRCCS Istituto Neurologico "Carlo Besta", Milan, Italy.
  • Sciacca FL; Laboratory of Clinical Investigation, Fondazione IRCCS Istituto Neurologico "Carlo Besta", Milan, Italy.
  • Broccoli V; Division of Neuroscience, San Raffaele Scientific Institute, Milan, Italy; National Research Council (CNR), Institute of Neuroscience, Milan, Italy.
  • Carelli V; IRCCS Istituto delle Scienze Neurologiche di Bologna, Bologna, Italy; Department of Biomedical and Neuromotor Sciences - DIBINEM, University of Bologna, Bologna, Italy.
  • Tiranti V; Unit of Medical Genetics and Neurogenetics, Fondazione IRCCS Istituto Neurologico "Carlo Besta", Milan, Italy. Electronic address: valeria.tiranti@istituto-besta.it.
Stem Cell Res ; 48: 101939, 2020 10.
Article em En | MEDLINE | ID: mdl-32771908
Assuntos
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Atrofia Óptica Hereditária de Leber / Células-Tronco Pluripotentes Induzidas Tipo de estudo: Risk_factors_studies Limite: Humans Idioma: En Revista: Stem Cell Res Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Itália
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Atrofia Óptica Hereditária de Leber / Células-Tronco Pluripotentes Induzidas Tipo de estudo: Risk_factors_studies Limite: Humans Idioma: En Revista: Stem Cell Res Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Itália