A Mouse Model of Familial Hypertrophic Cardiomyopathy von Anja A. T. Geisterfer-Lowrance, Christe, Michael, Conner, David A., Ingwall, Joanne S., Schoen, Frederick J., Seidman, Christine E., Seidman, J. G.

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A molecular basis for familial hypertrophic cardiomyopathy: A β cardiac myosin heavy chain gene missense mutation von Geisterfer-Lowrance, Anja A.T., Kass, Susan, Tanigawa, Gary, Vosberg, Hans-Peter, McKenna, William, Seidman, Christine E., Seidman, J.G.

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Production of homozygous mutant ES cells with a single targeting construct von MORTENSEN, RM, CONNER, DA, CHAO, S, GEISTERFERLOWRANCE, AAT, SEIDMAN, JG

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A locus for familial hypertrophic cardiomyopathy is closely linked to the cardiac myosin heavy chain genes, CRI-L436, and CRI-L329 on chromosome 14 at q11-q12 von SOLOMON, S. D, GEISTERFER-LOWRANCE, A. J. T, SEIDMAN, J. G, SEIDMAN, C. E, VOSBERG, H.-P, HILLER, G, JARCHO, J. A, MORTON, C. C, MCBRIDE, W. O, MITCHELL, A. L, BALE, A. E, MCKENNA, W. J

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