COL11A2 (Portuguese Wikipedia)

Analysis of information sources in references of the Wikipedia article "COL11A2" in Portuguese language version.

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Vuristo MM, Pihlajamaa T, Vandenberg P, Prockop DJ, Ala-Kokko L (setembro de 1995). «The human COL11A2 gene structure indicates that the gene has not evolved with the genes for the major fibrillar collagens». The Journal of Biological Chemistry. 270 (39): 22873–81. PMID 7559422. doi:10.1074/jbc.270.39.22873
McGuirt WT, Prasad SD, Griffith AJ, Kunst HP, Green GE, Shpargel KB, Runge C, Huybrechts C, Mueller RF, Lynch E, King MC, Brunner HG, Cremers CW, Takanosu M, Li SW, Arita M, Mayne R, Prockop DJ, Van Camp G, Smith RJ (dezembro de 1999). «Mutations in COL11A2 cause non-syndromic hearing loss (DFNA13)». Nature Genetics. 23 (4): 413–9. PMID 10581026. doi:10.1038/70516

«Human PubMed Reference:»
Vuristo MM, Pihlajamaa T, Vandenberg P, Prockop DJ, Ala-Kokko L (setembro de 1995). «The human COL11A2 gene structure indicates that the gene has not evolved with the genes for the major fibrillar collagens». The Journal of Biological Chemistry. 270 (39): 22873–81. PMID 7559422. doi:10.1074/jbc.270.39.22873
McGuirt WT, Prasad SD, Griffith AJ, Kunst HP, Green GE, Shpargel KB, Runge C, Huybrechts C, Mueller RF, Lynch E, King MC, Brunner HG, Cremers CW, Takanosu M, Li SW, Arita M, Mayne R, Prockop DJ, Van Camp G, Smith RJ (dezembro de 1999). «Mutations in COL11A2 cause non-syndromic hearing loss (DFNA13)». Nature Genetics. 23 (4): 413–9. PMID 10581026. doi:10.1038/70516
«Entrez Gene: COL11A2 collagen, type XI, alpha 2»