Identification of mutations in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricular cardiomyopathy type 2 (ARVD2)

By Bauce B.  

Human Molecular Genetics, Vol. 10, Iss. 3, 2001-02 ,pp. : 189-194

Oxford University Press

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Insertional mutation of the Attractin gene in the black tremor hamster

By Kuramoto Takashi   Nomoto Tomoko   Fujiwara Akira   Mizutani Makoto   Sugimura Takashi   Ushijima Toshikazu  

Mammalian Genome, Vol. 13, Iss. 1, 2002-01 ,pp. : 36-40

Springer Publishing Company

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Mutation at the anophthalmic white locus in Syrian hamsters: haploinsufficiency in the Mitf gene mimics human Waardenburg syndrome type 2

By Hodgkinson C.A.  

Human Molecular Genetics, Vol. 7, Iss. 4, 1998-04 ,pp. : 703-708

Oxford University Press

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Genetic variation in angiotensin-converting enzyme 2 gene is associated with extent of left ventricular hypertrophy in hypertrophic cardiomyopathy

By Merwe Lize   Cloete Ruben   Revera Miriam   Heradien Marshall   Goosen Althea   Corfield Valerie   Brink Paul   Moolman-Smook Johanna  

Human Genetics, Vol. 124, Iss. 1, 2008-08 ,pp. : 57-61

Springer Publishing Company

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Transthyretin gene V30M, H90N, and (del9) mutations in cardiomyopathy patients from St. Petersburg

By Solovyov K.   Grudinina N.   Semernin E.   Morozova I.   Smirnova S.   Polyakov D.   Aleynikova T.   Shliakhto E.   Gudkova A.   Shavlovsky M.  

Russian Journal of Genetics, Vol. 47, Iss. 4, 2011-04 ,pp. : 477-482

MAIK Nauka/Interperiodica

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