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Publications by Vincenzo Salpietro
Author Correction: Biallelic Expansion of an Intronic Repeat in RFC1 Is a Common Cause of Late-Onset Ataxia
Nature Genetics
Genetics
Biallelic Mutations in ADPRHL2, Encoding ADP-Ribosylhydrolase 3, Lead to a Degenerative Pediatric Stress-Induced Epileptic Ataxia Syndrome
American Journal of Human Genetics
Genetics
Mutations in ACTL6B Cause Neurodevelopmental Deficits and Epilepsy and Lead to Loss of Dendrites in Human Neurons
American Journal of Human Genetics
Genetics
Biallelic Mutations in ADPRHL2 , Encoding ADP-Ribosylhydrolase 3, Lead to a Degenerative Pediatric Stress-Induced Epileptic Ataxia Syndrome
American Journal of Human Genetics
Genetics
Cutis Tricolor: A Literature Review and Report of Five New Cases
Quantitative Imaging in Medicine and Surgery
Nuclear Medicine
Radiology
Imaging
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Putting Gene Essentiality Into Context
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Bayesian Molecular Clock Dating of Species Divergences in the Genomics Era
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