Akromatopsia (Estonian Wikipedia)

Analysis of information sources in references of the Wikipedia article "Akromatopsia" in Estonian language version.

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achromat.info

"www.achromat.info". Originaali arhiivikoopia seisuga 13. august 2009. Vaadatud 10. märtsil 2008.

Wissinger B, Gamer D, Jägle H; et al. (2001). "CNGA3 mutations in hereditary cone photoreceptor disorders". Am. J. Hum. Genet. 69 (4): 722–37. PMID 11536077. {{cite journal}}: et al.-i üleliigne kasutus kohas: |author= (juhend)CS1 hooldus: mitu nime: autorite loend (link)

Kohl S, Marx T, Giddings I; et al. (1998). "Total colourblindness is caused by mutations in the gene encoding the alpha-subunit of the cone photoreceptor cGMP-gated cation channel". Nat. Genet. 19 (3): 257–9. DOI:10.1038/935. PMID 9662398. {{cite journal}}: et al.-i üleliigne kasutus kohas: |author= (juhend)CS1 hooldus: mitu nime: autorite loend (link)

Johnson S, Michaelides M, Aligianis IA; et al. (2004). "Achromatopsia caused by novel mutations in both CNGA3 and CNGB3". J. Med. Genet. 41 (2): e20. PMID 14757870. {{cite journal}}: et al.-i üleliigne kasutus kohas: |author= (juhend)CS1 hooldus: mitu nime: autorite loend (link)
Wissinger B, Gamer D, Jägle H; et al. (2001). "CNGA3 mutations in hereditary cone photoreceptor disorders". Am. J. Hum. Genet. 69 (4): 722–37. PMID 11536077. {{cite journal}}: et al.-i üleliigne kasutus kohas: |author= (juhend)CS1 hooldus: mitu nime: autorite loend (link)
Kohl S, Marx T, Giddings I; et al. (1998). "Total colourblindness is caused by mutations in the gene encoding the alpha-subunit of the cone photoreceptor cGMP-gated cation channel". Nat. Genet. 19 (3): 257–9. DOI:10.1038/935. PMID 9662398. {{cite journal}}: et al.-i üleliigne kasutus kohas: |author= (juhend)CS1 hooldus: mitu nime: autorite loend (link)

"www.achromat.info". Originaali arhiivikoopia seisuga 13. august 2009. Vaadatud 10. märtsil 2008.