Literature DB >> 11157732

Lamin A/C gene mutation associated with dilated cardiomyopathy with variable skeletal muscle involvement.

H H Schmidt, H Lochs.   

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Year:  2001        PMID： 11157732     DOI： 10.1161/01.cir.103.4.e20

Source DB:  PubMed          Journal:  Circulation        ISSN： 0009-7322            Impact factor:   29.690


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  2 in total

1.  Meta-analysis of clinical characteristics of 299 carriers of LMNA gene mutations: do lamin A/C mutations portend a high risk of sudden death?

Authors:  Jop H van Berlo; Willem G de Voogt; Anneke J van der Kooi; J Peter van Tintelen; Gisèle Bonne; Rabah Ben Yaou; Denis Duboc; Tom Rossenbacker; Hein Heidbüchel; Marianne de Visser; Harry J G M Crijns; Yigal M Pinto
Journal:  J Mol Med (Berl)       Date:  2004-11-13       Impact factor: 4.599

2.  Identification of the molecular mechanisms underlying dilated cardiomyopathy via bioinformatic analysis of gene expression profiles.

Authors:  Hu Zhang; Zhuo Yu; Jianchao He; Baotong Hua; Guiming Zhang
Journal:  Exp Ther Med       Date:  2016-12-05       Impact factor: 2.447
  2 in total

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