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Date |
Item TypeArticle
A missense variant in desmoglein-2 predisposes to dilated cardiomyopathy.
Posch, M.G., Posch, M.J., Geier, C., Erdmann, B., Mueller, W., Richter, A., Ruppert, V., Pankuweit, S., Maisch, B., Perrot, A., Buttgereit, J., Dietz, R., Haverkamp, W. and Oezcelik, C.
Molecular Genetics and Metabolism 95
(1-2): 74-80.
September 2008
No evidence for an involvement of variants in the cannabinoid receptor gene (CNR1) in obesity in German children and adolescents.
Mueller, T.D., Reichwald, K., Wermter, A.K., Broenner, G., Nguyen, T.T., Friedel, S., Koberwitz, K., Engeli, S., Lichtner, P., Meitinger, T., Schaefer, H., Hebebrand, J. and Hinney, A.
Molecular Genetics and Metabolism 90
(4): 429-434.
April 2007
Letter
Mutations in MYOZ1 as well as MYOZ2 encoding the calsarcins are not associated with idiopathic and familial dilated cardiomyopathy.
Posch, M.G., Perrot, A., Dietz, R., Oezcelik, C., Pankuweit, S., Ruppert, V., Richter, A. and Maisch, B.
Molecular Genetics and Metabolism 91
(2): 207-208.
June 2007
Deletion of Glu at codon 13 in the TCAP gene encoding the Z-disc protein titin-cap/telethonin is a rare non-synonymous polymorphism.
Perrot, A., Posch, M.G. and Osterziel, K.J.
Molecular Genetics and Metabolism 88
(2): 199-200.
June 2006
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