LMOD3 (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "LMOD3" in English language version.

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doi.org

Gunning PW, Ghoshdastider U, Whitaker S, Popp D, Robinson RC (June 2015). "The evolution of compositionally and functionally distinct actin filaments". Journal of Cell Science. 128 (11): 2009–19. doi:10.1242/jcs.165563. PMID 25788699.
Nowak KJ, Davis MR, Wallgren-Pettersson C, Lamont PJ, Laing NG (November 2015). "Clinical utility gene card for: Nemaline myopathy - update 2015". European Journal of Human Genetics. 23 (11): 4–5. doi:10.1038/ejhg.2015.12. PMC 4613474. PMID 25712079.
Yuen M, Sandaradura SA, Dowling JJ, Kostyukova AS, Moroz N, Quinlan KG, et al. (November 2014). "Leiomodin-3 dysfunction results in thin filament disorganization and nemaline myopathy". The Journal of Clinical Investigation. 124 (11): 4693–708. doi:10.1172/JCI75199. PMC 4347224. PMID 25250574.

"Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
"Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
"Entrez Gene: LMOD3 leiomodin 3 (fetal)".
Nowak KJ, Davis MR, Wallgren-Pettersson C, Lamont PJ, Laing NG (November 2015). "Clinical utility gene card for: Nemaline myopathy - update 2015". European Journal of Human Genetics. 23 (11): 4–5. doi:10.1038/ejhg.2015.12. PMC 4613474. PMID 25712079.
Yuen M, Sandaradura SA, Dowling JJ, Kostyukova AS, Moroz N, Quinlan KG, et al. (November 2014). "Leiomodin-3 dysfunction results in thin filament disorganization and nemaline myopathy". The Journal of Clinical Investigation. 124 (11): 4693–708. doi:10.1172/JCI75199. PMC 4347224. PMID 25250574.

Gunning PW, Ghoshdastider U, Whitaker S, Popp D, Robinson RC (June 2015). "The evolution of compositionally and functionally distinct actin filaments". Journal of Cell Science. 128 (11): 2009–19. doi:10.1242/jcs.165563. PMID 25788699.
Nowak KJ, Davis MR, Wallgren-Pettersson C, Lamont PJ, Laing NG (November 2015). "Clinical utility gene card for: Nemaline myopathy - update 2015". European Journal of Human Genetics. 23 (11): 4–5. doi:10.1038/ejhg.2015.12. PMC 4613474. PMID 25712079.
Yuen M, Sandaradura SA, Dowling JJ, Kostyukova AS, Moroz N, Quinlan KG, et al. (November 2014). "Leiomodin-3 dysfunction results in thin filament disorganization and nemaline myopathy". The Journal of Clinical Investigation. 124 (11): 4693–708. doi:10.1172/JCI75199. PMC 4347224. PMID 25250574.