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1

Nanopore long-read next-generation sequencing for detection..:

Frascarelli, Chiara ; Zanetti, Nadia ; Nasca, Alessia...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10344361/. , 2023

Link: http://www.ncbi.nlm.nih...

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dateset relate to article (submitted) Evaluation of mitocho..:

Nasca, Alessia
doi:10.5281/zenodo.7937990. , 2023

Link: https://zenodo.org/recor..

3

Variants in ATP5F1B are associated with dominantly inherite..:

Nasca, Alessia ; Mencacci, Niccolò E ; Invernizzi, Federica...
info:eu-repo/semantics/altIdentifier/pmid/36860166. , 2023

Link: https://hdl.handle.net/2..

4

Expanding the spectrum of neonatal‐onset AIFM1‐associated d..:

Zambon, Alberto A ; Ghezzi, Daniele ; Baldoli, Cristina...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10578896/. , 2023

Link: http://www.ncbi.nlm.nih...

5

Variants in ATP5F1B are associated with dominantly inherite..:

Nasca, Alessia ; Mencacci, Niccolò E ; Invernizzi, Federica...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10316767/. , 2023

Link: http://www.ncbi.nlm.nih...

6

ENDOG_NGS data related to article "Biallelic variants in EN..:

Nasca, Alessia ; Legati, Andrea ; Ghezzi, Daniele
doi:10.5281/zenodo.6033814. , 2022

Link: https://zenodo.org/recor..

7

Biallelic Variants in ENDOG Associated with Mitochondrial M..:

Nasca, Alessia ; Legati, Andrea ; Meneri, Megi...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8946636/. , 2022

Link: http://www.ncbi.nlm.nih...

8

dataset related to article "Pathogenic variants in ATP5F1B ..:

Nasca, Alessia ; Ghezzi, Daniele
doi:10.5281/zenodo.6826777. , 2022

Link: https://zenodo.org/recor..

9

Myopathic mitochondrial DNA depletion syndrome associated w..:

Invernizzi, Federica ; Legati, Andrea ; Nasca, Alessia...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8536928/. , 2021

Link: http://www.ncbi.nlm.nih...

10

Novel NDUFA12 variants are associated with isolated complex..:

Torraco, Alessandra ; Nasca, Alessia ; Verrigni, Daniela...
https://discovery.ucl.ac.uk/id/eprint/10148272/1/humu.24195.pdf. , 2021

Link: https://discovery.ucl.ac..

11

Bi-allelic variants in OGDHL cause a neurodevelopmental spe..:

Yap, Zheng Yie ; Efthymiou, Stephanie ; Seiffert, Simone...
qt6480d7nc. , 2021

Link: https://escholarship.org..

12

Bi-allelic variants in OGDHL cause a neurodevelopmental spe..:

Yap, Zheng Yie ; Efthymiou, Stephanie ; Seiffert, Simone...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8715183/. , 2021

Link: http://www.ncbi.nlm.nih...

13

Novel deep intronic mutation in PLA2G6 causing early-onset ..:

Cavestro, Chiara ; Panteghini, Celeste ; Reale, Chiara...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8426226/. , 2021

Link: http://www.ncbi.nlm.nih...

14

ATPase Domain AFG3L2 Mutations Alter OPA1 Processing and Ca..:

Caporali, Leonardo ; Magri, Stefania ; Legati, Andrea...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7383914/. , 2020

Link: http://www.ncbi.nlm.nih...

15

Clinical-genetic features and peculiar muscle histopatholog..:

Verrigni, Daniela ; Nottia, Michela Di ; Ardissone, Anna...
info:eu-repo/semantics/altIdentifier/pmid/30801875. , 2019

Link: http://hdl.handle.net/24..

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