A cardiac myosin binding protein C mutation in the Maine Coon cat with familial hypertrophic cardiomyopathy

Author： Meurs Kathryn M.   Sanchez Ximena   David Ryan M.   Bowles Neil E.   Towbin Jeffrey A.   Reiser Peter J.   Kittleson Judith A.   Munro Marcia J.   Dryburgh Keith   MacDonald Kristin A.   Kittleson Mark D.  

Publisher： Oxford University Press

ISSN： 1460-2083

Source： Human Molecular Genetics, Vol.14, Iss.23, 2005-12, pp. : 3587-3593

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content

Expression of cardiac myosin-binding protein-C (cMyBP-C) in Drosophila as a model for the study of human cardiomyopathies

By Manh Thien Phong Vu  

Human Molecular Genetics, Vol. 14, Iss. 1, 2005-01 ,pp. : 7-17

Oxford University Press

Access to resources Recommend Favorite

Mutation of junctophilin type 2 associated with hypertrophic cardiomyopathy

By Matsushita Yoshihisa   Furukawa Toru   Kasanuki Hiroshi   Nishibatake Makoto   Kurihara Yachiyo   Ikeda Atsushi   Kamatani Naoyuki   Takeshima Hiroshi   Matsuoka Rumiko  

Journal of Human Genetics, Vol. 52, Iss. 6, 2007-06 ,pp. : 543-548

Springer Publishing Company

Access to resources Recommend Favorite

Mutations in the γ 2 subunit of AMP-activated protein kinase cause familial hypertrophic cardiomyopathy: evidence for the central role of energy compromise in disease pathogenesis

By Blair E.  

Human Molecular Genetics, Vol. 10, Iss. 11, 2001-05 ,pp. : 1215-1220

Oxford University Press

Access to resources Recommend Favorite

Isoleucyl-tRNA synthetase levels modulate the penetrance of a homoplasmic m.4277T>C mitochondrial tRNA Ile mutation causing hypertrophic cardiomyopathy

By Perli Elena   Giordano Carla   Tuppen Helen A.L.   Montopoli Monica   Montanari Arianna   Orlandi Maurizia   Pisano Annalinda   Catanzaro Daniela   Caparrotta Laura   Musumeci Beatrice   Autore Camillo   Morea Veronica   Di Micco Patrizio   Campese Antonio F.   Leopizzi Martina   Gallo Pietro   Francisci Silvia   Frontali Laura   Taylor Robert W.   d'Amati Giulia  

Human Molecular Genetics, Vol. 21, Iss. 1, 2012-01 ,pp. : 85-100

Oxford University Press

Access to resources Recommend Favorite

Myosin binding protein C1: a novel gene for autosomal dominant distal arthrogryposis type 1

By Gurnett Christina A.   Desruisseau David M.   McCall Kevin   Choi Ryan   Meyer Zachary I.   Talerico Michael   Miller Sara E.   Ju Jeong-Sun   Pestronk Alan   Connolly Anne M.   Druley Todd E.   Weihl Conrad C.   Dobbs Mathew B.  

Human Molecular Genetics, Vol. 19, Iss. 7, 2010-04 ,pp. : 1165-1173

Oxford University Press

Access to resources Recommend Favorite