Published March 24, 2021
| Version v1
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data related to article "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)"
Authors/Creators
- 1. Fondazione IRCCS - Istituto Neurologico Carlo Besta di Milano
Description
genetic analysis related to article "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)"
Notes
Study supported by: Italian Ministry of Health (Ricerca Finalizzata Grant: RF-2018-12366703) and MITOCON (Italian association for the study and treatment of Mithocondrial Diseases (Grant no. 2018-01)
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Additional details
Related works
- Is supplement to
- Journal article: 10.1016/j.scr.2020.101939 (DOI)