Molecular Genetics & Genomic Medicine (Jun 2021)
RNF213 variant in a patient with Legius syndrome associated with moyamoya syndrome
- Giulia Romanisio,
- Cristina Chelleri,
- Marcello Scala,
- Gianluca Piccolo,
- Barbara Carlini,
- Laura Gatti,
- Valeria Capra,
- Federico Zara,
- Anna Bersano,
- Marco Pavanello,
- Patrizia De Marco,
- Maria Cristina Diana
Affiliations
- Giulia Romanisio
- Pediatric Neurology and Neuromuscular Diseases Unit IRCCS Giannina Gaslini Institute Genoa Italy
- Cristina Chelleri
- Pediatric Neurology and Neuromuscular Diseases Unit IRCCS Giannina Gaslini Institute Genoa Italy
- Marcello Scala
- Pediatric Neurology and Neuromuscular Diseases Unit IRCCS Giannina Gaslini Institute Genoa Italy
- Gianluca Piccolo
- Pediatric Neurology and Neuromuscular Diseases Unit IRCCS Giannina Gaslini Institute Genoa Italy
- Barbara Carlini
- Medical Genetics Unit IRCCS Giannina Gaslini Institute Genoa Italy
- Laura Gatti
- Neurobiology Laboratory, Cerebrovascular Unit Fondazione IRCCS Istituto Neurologico Carlo Besta Milan Italy
- Valeria Capra
- Medical Genetics Unit IRCCS Giannina Gaslini Institute Genoa Italy
- Federico Zara
- Medical Genetics Unit IRCCS Giannina Gaslini Institute Genoa Italy
- Anna Bersano
- Cerebrovascular UnitFondazione IRCCS Istituto Neurologico Carlo Besta Milan Italy
- Marco Pavanello
- Pediatric Neurosurgery Unit IRCCS Giannina Gaslini Institute Genoa Italy
- Patrizia De Marco
- Medical Genetics Unit IRCCS Giannina Gaslini Institute Genoa Italy
- Maria Cristina Diana
- Pediatric Neurology and Neuromuscular Diseases Unit IRCCS Giannina Gaslini Institute Genoa Italy
- DOI
- https://doi.org/10.1002/mgg3.1669
- Journal volume & issue
-
Vol. 9,
no. 6
pp. n/a – n/a
Abstract
No abstracts available.
