Expanding the Clinical Spectrum of DRP2 -Associated Charcot-Marie-Tooth Disease.

Fecha de publicación:

Autores de CIPF

Participantes ajenos a CIPF

  • Sivera R
  • Pelayo-Negro AL
  • Jericó I
  • Domínguez-González C
  • Horga A
  • Rodriguez De Rivera FJ
  • Gallardo E
  • Tembl JI
  • Bermejo-Guerrero L
  • Pagola Lorz MI
  • Azorín I
  • Cordoba M
  • Fenollar-Cortés MDM
  • Millet E
  • Vilchez JJ
  • Apellániz-Ruiz M
  • Sevilla T

Grupos de Investigación

Abstract

Germline truncating variants in the DRP2 gene (encoding dystrophin-related protein 2) cause the disruption of the periaxin-DRP2-dystroglycan complex and have been linked to Charcot-Marie-Tooth disease. However, the causality and the underlying phenotype of the genetic alterations are not clearly defined.

Datos de la publicación

ISSN/ISSNe:
0028-3878, 1526-632X

NEUROLOGY  LIPPINCOTT WILLIAMS & WILKINS

Tipo:
Article
Páginas:
-
PubMed:
38513194

Citas Recibidas en Web of Science: 1

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