LCA5 (Portuguese Wikipedia)

Analysis of information sources in references of the Wikipedia article "LCA5" in Portuguese language version.

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Dharmaraj S, Li Y, Robitaille JM, Silva E, Zhu D, Mitchell TN, Maltby LP, Baffoe-Bonnie AB, Maumenee IH (janeiro de 2000). «A novel locus for Leber congenital amaurosis maps to chromosome 6q». Am. J. Hum. Genet. 66 (1): 319–26. PMC 1288337. PMID 10631161. doi:10.1086/302719
den Hollander AI, Koenekoop RK, Mohamed MD, Arts HH, Boldt K, Towns KV, Sedmak T, Beer M, Nagel-Wolfrum K, McKibbin M, Dharmaraj S, Lopez I, Ivings L, Williams GA, Springell K, Woods CG, Jafri H, Rashid Y, Strom TM, van der Zwaag B, Gosens I, Kersten FF, van Wijk E, Veltman JA, Zonneveld MN, van Beersum SE, Maumenee IH, Wolfrum U, Cheetham ME, Ueffing M, Cremers FP, Inglehearn CF, Roepman R (julho de 2007). «Mutations in LCA5, encoding the ciliary protein lebercilin, cause Leber congenital amaurosis». Nat. Genet. 39 (7): 889–95. PMID 17546029. doi:10.1038/ng2066

«Human PubMed Reference:»
«Entrez Gene: Leber congenital amaurosis 5»
Dharmaraj S, Li Y, Robitaille JM, Silva E, Zhu D, Mitchell TN, Maltby LP, Baffoe-Bonnie AB, Maumenee IH (janeiro de 2000). «A novel locus for Leber congenital amaurosis maps to chromosome 6q». Am. J. Hum. Genet. 66 (1): 319–26. PMC 1288337. PMID 10631161. doi:10.1086/302719
den Hollander AI, Koenekoop RK, Mohamed MD, Arts HH, Boldt K, Towns KV, Sedmak T, Beer M, Nagel-Wolfrum K, McKibbin M, Dharmaraj S, Lopez I, Ivings L, Williams GA, Springell K, Woods CG, Jafri H, Rashid Y, Strom TM, van der Zwaag B, Gosens I, Kersten FF, van Wijk E, Veltman JA, Zonneveld MN, van Beersum SE, Maumenee IH, Wolfrum U, Cheetham ME, Ueffing M, Cremers FP, Inglehearn CF, Roepman R (julho de 2007). «Mutations in LCA5, encoding the ciliary protein lebercilin, cause Leber congenital amaurosis». Nat. Genet. 39 (7): 889–95. PMID 17546029. doi:10.1038/ng2066