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Doriana Sandonà
Doriana Sandonà
Biology
Molecular biology
Nuclear gene
SURF1
Genetics
4
Papers
313
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0.01
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Different outcome of sarcoglycan missense mutation between human and mouse.
2018
PLOS ONE
Sara F Henriques
Cécile Patissier
Nathalie Bourg
Chiara Fecchio
Doriana Sandonà
Justine Marsolier
Isabelle Richard
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Citations (8)
Trophic activity of a naturally occurring truncated isoform of the P2X7 receptor
2010
The FASEB Journal
Elena Adinolfi
Maria Cirillo
Ronja Woltersdorf
Simonetta Falzoni
Paola Chiozzi
Patrizia Pellegatti
Maria Giulia Callegari
Doriana Sandonà
Fritz Markwardt
Günther Schmalzing
Francesco Di Virgilio
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Citations (174)
A Single Cell Complementation Class is Common to Several Cases of Cytochrome c Oxidase-Defective Leigh's Syndrome
1997
Human Molecular Genetics
Monica Munaro
Valeria Tiranti
Doriana Sandonà
Eleonora Lamantea
Graziella Uziel
Roberto Bisson
Massimo Zeviani
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Citations (53)
Nuclear DNA origin of cytochrome c oxidase deficiency in Leigh's syndrome: genetic evidence based on patient's-derived rho° transformants
1995
Human Molecular Genetics
Valeria Tiranti
Monica Munaro
Doriana Sandonà
Eleonora Lamantea
M. Rimoldi
Stefano DiDonato
Roberto Bisson
Massimo Zeviani
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Citations (78)
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