Expanding the phenotypic spectrum of BCS1L‐related mitochondrial disease

OBJECTIVE: To delineate the full phenotypic spectrum of BCS1L‐related disease, provide better understanding of the genotype–phenotype correlations and identify reliable prognostic disease markers. METHODS: We performed a retrospective multinational cohort study of previously unpublished patients fol...

Descripción completa

Detalles Bibliográficos
Autores principales: Hikmat, Omar, Isohanni, Pirjo, Keshavan, Nandaki, Ferla, Matteo P., Fassone, Elisa, Abbott, Mary‐Alice, Bellusci, Marcello, Darin, Niklas, Dimmock, David, Ghezzi, Daniele, Houlden, Henry, Invernizzi, Federica, Kamarus Jaman, Nazreen B., Kurian, Manju A., Morava, Eva, Naess, Karin, Ortigoza‐Escobar, Juan Darío, Parikh, Sumit, Pennisi, Alessandra, Barcia, Giulia, Tylleskär, Karin B., Brackman, Damien, Wortmann, Saskia B., Taylor, Jenny C., Bindoff, Laurence A., Fellman, Vineta, Rahman, Shamima
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8607453/
https://www.ncbi.nlm.nih.gov/pubmed/34662929
http://dx.doi.org/10.1002/acn3.51470

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8607453/
https://www.ncbi.nlm.nih.gov/pubmed/34662929
http://dx.doi.org/10.1002/acn3.51470

Ejemplares similares