Generation of two human iPSC lines, FINCBi002-A and FINCBi003-A, carrying heteroplasmic macrodeletion of mitochondrial DNA causing Pearson's syndrome.

Peron, Camille; Mauceri, Roberta; Iannielli, Angelo; Cavaliere, Andrea; Legati, Andrea; Rizzo, Ambra; Sciacca, Francesca L; Broccoli, Vania; Tiranti, Valeria

Peron, Camille; Mauceri, Roberta; Iannielli, Angelo; Cavaliere, Andrea; Legati, Andrea; Rizzo, Ambra; Sciacca, Francesca L; Broccoli, Vania; Tiranti, Valeria.

Afiliación

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.
Iannielli A; San Raffaele Scientific Institute, Milan, Italy; National Research Council (CNR), Institute of Neuroscience, Milan, Italy.
Cavaliere A; Unit of Medical Genetics and Neurogenetics, Fondazione IRCCS Istituto Neurologico "Carlo Besta", Milan, Italy.
Legati A; Unit of Medical Genetics and Neurogenetics, Fondazione IRCCS Istituto Neurologico "Carlo Besta", 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; San Raffaele Scientific Institute, Milan, Italy; National Research Council (CNR), Institute of Neuroscience, Milan, 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 ; 50: 102151, 2021 Jan 04.

Article en En | MEDLINE | ID: mdl-33434818

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Stem Cell Res Año: 2021 Tipo del documento: Article País de afiliación: Italia Pais de publicación: Reino Unido

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