Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Niccolò N. Vanni"'
Autor:
Greta Rossi, Gabriele Ordazzo, Niccolò N Vanni, Valerio Castoldi, Angelo Iannielli, Dario Di Silvestre, Edoardo Bellini, Letizia Bernardo, Serena G Giannelli, Mirko Luoni, Sharon Muggeo, Letizia Leocani, PierLuigi Mauri, Vania Broccoli
Publikováno v:
eLife, Vol 12 (2023)
Wolfram syndrome 1 (WS1) is a rare genetic disorder caused by mutations in the WFS1 gene leading to a wide spectrum of clinical dysfunctions, among which blindness, diabetes, and neurological deficits are the most prominent. WFS1 encodes for the endo
Externí odkaz:
https://doaj.org/article/587df71ad8444471a703dfcbc9ffb880
Autor:
Greta Rossi, Gabriele Ordazzo, Niccolò N Vanni, Valerio Castoldi, Angelo Iannielli, Dario Di Silvestre, Edoardo Bellini, Letizia Bernardo, Serena G Giannelli, Mirko Luoni, Sharon Muggeo, Letizia Leocani, PierLuigi Mauri, Vania Broccoli
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::75b34de2a124ad5445b13280c9194419
https://doi.org/10.7554/elife.81779.sa2
https://doi.org/10.7554/elife.81779.sa2
Autor:
Greta Rossi, Gabriele Ordazzo, Niccolò N. Vanni, Valerio Castoldi, Angelo Iannielli, Dario Di Silvestre, Edoardo Bellini, Letizia Bernardo, Serena G. Giannelli, Sharon Muggeo, Leocani Letizia, PierLuigi Mauri, Vania Broccoli
SummaryWolfram syndrome 1 (WS1) is a rare genetic disorder caused by mutations in the WFS1 gene leading to a wide spectrum of clinical dysfunctions, among which blindness, diabetes and neurological deficits are the most prominent. WFS1 encodes for th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3bc51958bd37c393ac9b088331638440
https://doi.org/10.1101/2022.07.18.500452
https://doi.org/10.1101/2022.07.18.500452