Confirmation of the Pathogenetic Role of the <scp><i>CCDC88C</i></scp> Gene in Early‐Onset Pure Spastic Paraplegia-Reference-Cited by-同舟云学术

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Confirmation of the Pathogenetic Role of the CCDC88C Gene in Early‐Onset Pure Spastic Paraplegia

Published:2023-06-15 Issue:8 Volume:38 Page:1561-1562
ISSN:0885-3185
Container-title:Movement Disorders
language:en
Short-container-title:Movement Disorders

Author:

Caputo Donatella¹,Cetica Valentina¹,Paoli Silvia²,Rosati Anna¹^ORCID,Lazzeri Simone³

Affiliation:

1. Neuroscience Department Meyer Children's Hospital IRCCS, University of Florence Florence Italy

2. Department of Physical Medicine and Rehabilitation Meyer Children's Hospital IRCCS, University of Florence Florence Italy

3. Pediatric Orthopedics Unit APSS Santa Chiara Hospital Trento Italy

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Reference7 articles.

1. Hereditary spastic paraplegia

2. Converging cellular themes for the hereditary spastic paraplegias

3. A heterozygous mutation in the CCDC88C gene likely causes early-onset pure hereditary spastic paraplegia: a case report

4. Identification and characterization of a novel Dvl-binding protein that suppresses Wnt signalling pathway

5. A novel missense mutation inCCDC88Cactivates the JNK pathway and causes a dominant form of spinocerebellar ataxia

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