RYR1 c.10348-6C>G

Variant ID: 19-39013851-C-G

NM_000540.2(RYR1):c.10348-6C>G

This variant was identified in 1 publication

View GRCh38 version.




Publications:


'Dusty core disease' (DuCD): expanding morphological spectrum of RYR1 recessive myopathies.

Acta Neuropathologica Communications
Garibaldi, Matteo M; Rendu, John J; Brocard, Julie J; Lacene, Emmanuelle E; Fauré, Julien J; Brochier, Guy G; Beuvin, Maud M; Labasse, Clemence C; Madelaine, Angeline A; Malfatti, Edoardo E; Bevilacqua, Jorge Alfredo JA; Lubieniecki, Fabiana F; Monges, Soledad S; Taratuto, Ana Lia AL; Laporte, Jocelyn J; Marty, Isabelle I; Antonini, Giovanni G; Romero, Norma Beatriz NB
Publication Date: 2019-01-05

Variant appearance in text: RYR1: 10348-6C>G; rs193922837
PubMed Link: 30611313
Variant Present in the following documents:
  • 40478_2018_655_MOESM1_ESM.xlsx, sheet 8
  • 40478_2018_655_MOESM1_ESM.xlsx, sheet 7
  • 40478_2018_655_MOESM1_ESM.xlsx, sheet 6
  • 40478_2018_655_MOESM1_ESM.xlsx, sheet 3
  • 40478_2018_655_MOESM1_ESM.xlsx, sheet 1
View BVdb publication page