Literature DB >> 7848441

A new missense mutation, Arg719Gln, in the beta-cardiac heavy chain myosin gene of patients with familial hypertrophic cardiomyopathy.

M W Consevage1, G C Salada, B G Baylen, R L Ladda, P K Rogan.   

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Year:  1994        PMID： 7848441     DOI： 10.1093/hmg/3.6.1025

Source DB:  PubMed          Journal:  Hum Mol Genet        ISSN： 0964-6906            Impact factor:   6.150


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  11 in total

1.  From malignant mutations to malignant domains: the continuing search for prognostic significance in the mutant genes causing hypertrophic cardiomyopathy.

Authors:  S L Van Driest; B J Maron; M J Ackerman
Journal:  Heart       Date:  2004-01       Impact factor: 5.994

2.  Founder mutations in hypertrophic cardiomyopathy patients in the Netherlands.

Authors:  I Christiaans; E A Nannenberg; D Dooijes; R J E Jongbloed; M Michels; P G Postema; D Majoor-Krakauer; A van den Wijngaard; M M A M Mannens; J P van Tintelen; I M van Langen; A A M Wilde
Journal:  Neth Heart J       Date:  2010-05       Impact factor: 2.380

3.  Characterization of mutant myosins of Dictyostelium discoideum equivalent to human familial hypertrophic cardiomyopathy mutants. Molecular force level of mutant myosins may have a prognostic implication.

Authors:  H Fujita; S Sugiura; S Momomura; M Omata; H Sugi; K Sutoh
Journal:  J Clin Invest       Date:  1997-03-01       Impact factor: 14.808

4.  Prognostic predictive value of gene mutations in Japanese patients with hypertrophic cardiomyopathy.

Authors:  Ayako Chida; Kei Inai; Hiroki Sato; Eriko Shimada; Tsutomu Nishizawa; Mitsuyo Shimada; Michiko Furutani; Yoshiyuki Furutani; Yoichi Kawamura; Masaya Sugimoto; Jun Ishihara; Masako Fujiwara; Takashi Soga; Masatoshi Kawana; Shinya Fuji; Shigeru Tateno; Kenji Kuraishi; Shigetoyo Kogaki; Mitsuhiro Nishimura; Mamoru Ayusawa; Fukiko Ichida; Hirokuni Yamazawa; Rumiko Matsuoka; Shigeaki Nonoyama; Toshio Nakanishi
Journal:  Heart Vessels       Date:  2016-11-24       Impact factor: 2.037

Review 5.  Mutation type is not clinically useful in predicting prognosis in hypertrophic cardiomyopathy.

Authors:  Andrew P Landstrom; Michael J Ackerman
Journal:  Circulation       Date:  2010-12-07       Impact factor: 29.690

6.  The origins of hypertrophic cardiomyopathy-causing mutations in two South African subpopulations: a unique profile of both independent and founder events.

Authors:  J C Moolman-Smook; W J De Lange; E C Bruwer; P A Brink; V A Corfield
Journal:  Am J Hum Genet       Date:  1999-11       Impact factor: 11.025

7.  Serial observations and mutational analysis of an adoptee with family history of hypertrophic cardiomyopathy.

Authors:  Bronwyn Harris; Jean P Pfotenhauer; Cheri A Silverstein; Larry W Markham; Kim Schafer; Vernat J Exil; Charles C Hong
Journal:  Cardiol Res Pract       Date:  2010-03-11       Impact factor: 1.866

8.  Shared genetic causes of cardiac hypertrophy in children and adults.

Authors:  Hiroyuki Morita; Heidi L Rehm; Andres Menesses; Barbara McDonough; Amy E Roberts; Raju Kucherlapati; Jeffrey A Towbin; J G Seidman; Christine E Seidman
Journal:  N Engl J Med       Date:  2008-04-09       Impact factor: 91.245

9.  Structural interpretation of the mutations in the beta-cardiac myosin that have been implicated in familial hypertrophic cardiomyopathy.

Authors:  I Rayment; H M Holden; J R Sellers; L Fananapazir; N D Epstein
Journal:  Proc Natl Acad Sci U S A       Date:  1995-04-25       Impact factor: 11.205

10.  Early results of sarcomeric gene screening from the Egyptian National BA-HCM Program.

Authors:  Heba Sh Kassem; Remon S Azer; Maha Saber-Ayad; Maha S Ayad; Sarah Moharem-Elgamal; Gehan Magdy; Ahmed Elguindy; Franco Cecchi; Iacopo Olivotto; Magdi H Yacoub
Journal:  J Cardiovasc Transl Res       Date:  2012-12-12       Impact factor: 4.132
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