WASHC5 (Spanish Wikipedia)

Analysis of information sources in references of the Wikipedia article "WASHC5" in Spanish language version.

Last modified: 15:17:36, 6 November 2025 (UTC)

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5^th place

33^rd place

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2^nd place

10^th place

253^rd place

low place

doi.org (Global: 2^nd place; Spanish: 2^nd place)

Seaman, Matthew N. J.; Gautreau, Alexis; Billadeau, Daniel D. (1 de noviembre de 2013). «Retromer-mediated endosomal protein sorting: all WASHed up!». Trends in Cell Biology 23 (11): 522-528. ISSN 1879-3088. PMC 3924425. PMID 23721880. doi:10.1016/j.tcb.2013.04.010.
Jahic, Amir; Khundadze, Mukhran; Jaenisch, Nadine; Schüle, Rebecca; Klimpe, Sven; Klebe, Stephan; Frahm, Christiane; Kassubek, Jan et al. (16 de noviembre de 2015). «The spectrum of KIAA0196 variants, and characterization of a murine knockout: implications for the mutational mechanism in hereditary spastic paraplegia type SPG8». Orphanet Journal of Rare Diseases (en inglés) 10 (1). ISSN 1750-1172. PMC 4647479. PMID 26572744. doi:10.1186/s13023-015-0359-x.

Seaman, Matthew N. J.; Gautreau, Alexis; Billadeau, Daniel D. (1 de noviembre de 2013). «Retromer-mediated endosomal protein sorting: all WASHed up!». Trends in Cell Biology 23 (11): 522-528. ISSN 1879-3088. PMC 3924425. PMID 23721880. doi:10.1016/j.tcb.2013.04.010.
Jahic, Amir; Khundadze, Mukhran; Jaenisch, Nadine; Schüle, Rebecca; Klimpe, Sven; Klebe, Stephan; Frahm, Christiane; Kassubek, Jan et al. (16 de noviembre de 2015). «The spectrum of KIAA0196 variants, and characterization of a murine knockout: implications for the mutational mechanism in hereditary spastic paraplegia type SPG8». Orphanet Journal of Rare Diseases (en inglés) 10 (1). ISSN 1750-1172. PMC 4647479. PMID 26572744. doi:10.1186/s13023-015-0359-x.