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.