Condition: Malouf syndrome


rs58922911 in LMNA gene and Malouf syndrome PMID 17150192 2007 Collagen expression in fibroblasts with a novel LMNA mutation.

PMID 12927431 2003 LMNA mutations in atypical Werner's syndrome.

PMID 19283854 2009 Ovarian failure and dilated cardiomyopathy due to a novel lamin mutation.