High mutation detection rate in the COL4A5 collagen gene in suspected Alport syndrome using PCR and direct DNA sequencing von MARTIN, P, HEISKARI, N, NEUMANN, H, SPRINGATE, J, SHOWS, T, PETTERSSON, E, TRYGGVASON, K, JING ZHOU, LEINONEN, A, TUMELIUS, T, HERTZ, J. M, BARKER, D, GREGORY, M, ATKIN, C, STYRKARSDOTTIR, U

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X-linked alport syndrome : an SSCP-based mutation survey over all 51 exons of the COL4A5 gene von RENIERI, A, BRUTTINI, M, MASSELLA, L, BANFI, G, SCOLARI, F, SESSA, A, RIZZONI, G, TRYGGVASON, K, PIGNATTI, P. F, SAVI, M, BALLABIO, A, DE MARCHI, M, GALLI, L, ZANELLI, P, NERI, T, ROSSETTI, S, TURCO, A, HEISKARI, N, ZHOU, J, GUSMANO, R

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Spectrum of COL4A5 mutations in Finnish Alport syndrome patients von Martin, Paula, Heiskari, Niina, Pajari, Heli, Grönhagen-Riska, Carola, Kääriäinen, Helena, Koskimies, Olli, Tryggvason, Karl

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Identification of 17 mutations in ten exons in the COL4A5 collagen gene, but no mutations found in four exons in COL4A6: a study of 250 patients with hematuria and suspected of hav... von Heiskari, N, Zhang, X, Zhou, J, Leinonen, A, Barker, D, Gregory, M, Atkin, C L, Netzer, K O, Weber, M, Reeders, S, Grönhagen-Riska, C, Neumann, H P, Trembath, R, Tryggvason, K

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Ocular findings in 34 patients with Alport syndrome, correlation of the findings to mutations in COL4A5 gene von Pajari, H., Setälä, K., Heiskari, N., Kääriäinen, H., Rosenlöf, K., Koskimies, O.

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A nonsense mutation in the COL4A5 collagen gene in a family with X-linked juvenile Alport syndrome von Hertz, Jens Michael, Heiskari, Niina, Zhou, Jing, Jensen, Uffe Birk, Tryggvason, Karl

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