<scp><i>BCL11B</i></scp>‐Related Dystonia: Further Evidence of an Emerging Cause of Childhood‐Onset Generalized Dystonia-Reference-Cited by-同舟云学术

BCL11B‐Related Dystonia: Further Evidence of an Emerging Cause of Childhood‐Onset Generalized Dystonia

Published:2024-05-27 Issue:7 Volume:11 Page:897-901
ISSN:2330-1619
Container-title:Movement Disorders Clinical Practice
language:en
Short-container-title:Movement Disord Clin Pract

Author:

Garone Giacomo¹²^ORCID,Capuano Alessandro³,Amodio Donato⁴,Nicita Francesco⁵,Travaglini Lorena⁶,Graziola Federica⁷^ORCID,De Benedictis Alessandro⁸,Frascarelli Flaminia⁹,Parisi Pasquale²,Pizzi Simone¹⁰,Tartaglia Marco¹⁰,Marras Carlo Efisio⁸,Niceta Marcello¹⁰

Affiliation:

1. Neurology, Epilepsy and Movement Disorders Unit Bambino Gesù Children's Hospital, IRCCS Rome Italy

2. Department of Neuroscience, Mental Health and Sensory Organs (NESMOS), Faculty of Medicine and Psychology Sapienza University of Rome Rome Italy

3. Child and Adolescent Neuropsychiatric Unit, Azienda Sanitaria Locale Viterbo Viterbo Italy

4. Academic Department of Pediatrics (DPUO), Research Unit of Clinical Immunology and Vaccinology Bambino Gesù Children's Hospital, IRCCS Rome Italy

5. Genetics and Rare Diseases Research Division, Unit of Neuromuscular and Neurodegenerative Disorders Bambino Gesù Children's Hospital, IRCCS Rome Italy

6. Laboratory of Medical Genetics Bambino Gesù Children's Hospital, IRCCS Rome Italy

7. Department of Paediatric Neuroscience Fondazione IRCCS Istituto Neurologico Carlo Besta Milan Italy

8. Neurosurgery Unit Bambino Gesù Children's Hospital, IRCCS Rome Italy

9. Neurorehabilitation Unit Bambino Gesù Children's Hospital Rome Italy

10. Genetics and Rare Diseases Research Division Bambino Gesù Children's Hospital, IRCCS Rome Italy

Publisher

Wiley

Reference10 articles.

1. Bcl11b—A Critical Neurodevelopmental Transcription Factor—Roles in Health and Disease

2. BCL11B mutations in patients affected by a neurodevelopmental disorder with reduced type 2 innate lymphoid cells

4. In-depth analysis reveals complex molecular aetiology in a cohort of idiopathic cerebral palsy

5. A de novo BCL11B variant case manifesting with dystonic movement disorder regarding the article “BCL11B-related disorder in two canadian children: Expanding the clinical phenotype (Prasad et al., 2020).”