Pediatric Dilated Cardiomyopathy‐Associated LRRC10 (Leucine‐Rich Repeat–Containing 10) Variant Reveals LRRC10 as an Auxiliary Subunit of Cardiac L‐Type Ca(2+) Channels

BACKGROUND: Genetic causes of dilated cardiomyopathy (DCM) are incompletely understood. LRRC10 (leucine‐rich repeat–containing 10) is a cardiac‐specific protein of unknown function. Heterozygous mutations in LRRC10 have been suggested to cause DCM, and deletion of Lrrc10 in mice results in DCM. METH...

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Detalles Bibliográficos
Autores principales: Woon, Marites T., Long, Pamela A., Reilly, Louise, Evans, Jared M., Keefe, Alexis M., Lea, Martin R., Beglinger, Carl J., Balijepalli, Ravi C., Lee, Youngsook, Olson, Timothy M., Kamp, Timothy J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Original Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5850229/
https://www.ncbi.nlm.nih.gov/pubmed/29431102
http://dx.doi.org/10.1161/JAHA.117.006428

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5850229/
https://www.ncbi.nlm.nih.gov/pubmed/29431102
http://dx.doi.org/10.1161/JAHA.117.006428

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