Ovarian failure and dilated cardiomyopathy due to a novel lamin mutation
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.32627/fullpdf
Reference12 articles.
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2. LMNA mutations in atypical Werner's syndrome;Chen;Lancet,2003
3. Multisystem dystrophy syndrome due to novel missense mutations in the amino-terminal head and alpha-helical rod domains of the lamin A/C gene;Garg;Am J Med,2002
4. Familial dilated cardiomyopathy hypergonadotrophic hypogonadism associated with thyroid hemiagenesis;Gursoy;Am J Med Genet Part A,2006
5. p.S143F mutation in lamin A/C: A new phenotype combining myopathy and progeria;Kirschner;Ann Neurol,2005
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