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IFT80 (Persian Wikipedia)

Analysis of information sources in references of the Wikipedia article "IFT80" in Persian language version.

Last modified:

Ref.Un. Ref.Website
Global rank Persian rank
64nih.gov
5th place
3rd place
62ensembl.org
630th place
387th place
21doi.org
2nd place
2nd place

doi.org (Global: 2nd place; Persian: 2nd place)

  • Beales PL, Bland E, Tobin JL, Bacchelli C, Tuysuz B, Hill J, Rix S, Pearson CG, Kai M, Hartley J, Johnson C, Irving M, Elcioglu N, Winey M, Tada M, Scambler PJ (June 2007). "IFT80, which encodes a conserved intraflagellar transport protein, is mutated in Jeune asphyxiating thoracic dystrophy". Nat. Genet. 39 (6): 727–9. doi:10.1038/ng2038. PMID 17468754.

ensembl.org (Global: 630th place; Persian: 387th place)

may2017.archive.ensembl.org

nih.gov (Global: 5th place; Persian: 3rd place)

ncbi.nlm.nih.gov

pubmed.ncbi.nlm.nih.gov

  • Beales PL, Bland E, Tobin JL, Bacchelli C, Tuysuz B, Hill J, Rix S, Pearson CG, Kai M, Hartley J, Johnson C, Irving M, Elcioglu N, Winey M, Tada M, Scambler PJ (June 2007). "IFT80, which encodes a conserved intraflagellar transport protein, is mutated in Jeune asphyxiating thoracic dystrophy". Nat. Genet. 39 (6): 727–9. doi:10.1038/ng2038. PMID 17468754.