Clinical, histological and genetic characterisation of patients with tubular aggregate myopathy caused by mutations in STIM1-Reference-Cited by-同舟云学术

Clinical, histological and genetic characterisation of patients with tubular aggregate myopathy caused by mutations in STIM1

Published:2014-10-17 Issue:12 Volume:51 Page:824-833
ISSN:0022-2593
Container-title:Journal of Medical Genetics
language:en
Short-container-title:J Med Genet

Author:

Böhm Johann,Chevessier Frédéric,Koch Catherine,Peche G Arielle,Mora Marina,Morandi Lucia,Pasanisi Barbara,Moroni Isabella,Tasca Giorgio,Fattori Fabiana,Ricci Enzo,Pénisson-Besnier Isabelle,Nadaj-Pakleza Aleksandra,Fardeau Michel,Joshi Pushpa Raj,Deschauer Marcus,Romero Norma Beatriz,Eymard Bruno,Laporte Jocelyn

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference27 articles.

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3. Structural and mechanistic insights into STIM1-mediated initiation of store-operated calcium entry;Stathopulos;Cell,2008

4. Stored Ca2+ depletion-induced oligomerization of stromal interaction molecule 1 (STIM1) via the EF-SAM region: an initiation mechanism for capacitive Ca2+ entry;Stathopulos;J Biol Chem,2006

5. STIM1 is a Ca2+ sensor that activates CRAC channels and migrates from the Ca2+ store to the plasma membrane;Zhang;Nature,2005

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