FSCN2 (Russian Wikipedia)

Analysis of information sources in references of the Wikipedia article "FSCN2" in Russian language version.

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Bardien-Kruger S., Greenberg J., Tubb B., Bryan J., Queimado L., Lovett M., Ramesar R.S. Refinement of the RP17 locus for autosomal dominant retinitis pigmentosa, construction of a YAC contig and investigation of the candidate gene retinal fascin (англ.) // Eur J Hum Genet^[англ.] : journal. — 1999. — June (vol. 7, no. 3). — P. 332—338. — doi:10.1038/sj.ejhg.5200302. — PMID 10234509.

Bardien-Kruger S., Greenberg J., Tubb B., Bryan J., Queimado L., Lovett M., Ramesar R.S. Refinement of the RP17 locus for autosomal dominant retinitis pigmentosa, construction of a YAC contig and investigation of the candidate gene retinal fascin (англ.) // Eur J Hum Genet^[англ.] : journal. — 1999. — June (vol. 7, no. 3). — P. 332—338. — doi:10.1038/sj.ejhg.5200302. — PMID 10234509.
Entrez Gene: FSCN2 fascin homolog 2, actin-bundling protein, retinal (Strongylocentrotus purpuratus) (неопр.). Архивировано 5 декабря 2010 года.

Bardien-Kruger S., Greenberg J., Tubb B., Bryan J., Queimado L., Lovett M., Ramesar R.S. Refinement of the RP17 locus for autosomal dominant retinitis pigmentosa, construction of a YAC contig and investigation of the candidate gene retinal fascin (англ.) // Eur J Hum Genet^[англ.] : journal. — 1999. — June (vol. 7, no. 3). — P. 332—338. — doi:10.1038/sj.ejhg.5200302. — PMID 10234509.