Lucia Perone
Pozzuoli, Italy
Last Updated: 09/26/2026
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Found 8 publications
Author Correction: Characterization of the most frequent ATP7B mutation causing Wilson disease in hepatocytes from patient induced pluripotent stem cells.
Journal: Scientific reports
Published: June 24, 2020
Trans-generational epigenetic regulation associated with the amelioration of Duchenne Muscular Dystrophy.
Journal: EMBO molecular medicine
Published: January 22, 2020
Characterization of the most frequent ATP7B mutation causing Wilson disease in hepatocytes from patient induced pluripotent stem cells.
Journal: Scientific reports
Published: January 22, 2018
Multiplex Ligation-Dependent Probe Amplification Accurately Detects Turner Syndrome in Girls with Short Stature.
Journal: Hormone research in paediatrics
Published: June 20, 2016
Two maternal duplications involving the CDKN1C gene are associated with contrasting growth phenotypes.
Journal: Clinical epigenetics
Published: April 07, 2016
MePR: a novel human mesenchymal progenitor model with characteristics of pluripotency.
Journal: Stem cells and development
Published: April 20, 2013
Familial trisomy 6p in mother and daughter.
Journal: American journal of medical genetics. Part A
Published: April 10, 2012
Showing 1-8 of 8
Last Updated: 09/26/2026