Source: ORPHANET

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4000
Gene Symbol: LMNA
LMNA
CUI: C4275075
Disease: Atypical Werner syndrome
Atypical Werner syndrome 		0.400 GermlineCausalMutation ORPHANET Novel LMNA gene mutation in a patient with Atypical Werner's Syndrome. 19270485

2009
Entrez Id: 4000
Gene Symbol: LMNA
LMNA
CUI: C4275075
Disease: Atypical Werner syndrome
Atypical Werner syndrome 		0.400 GermlineCausalMutation ORPHANET In four (15%) of 26 patients with atypical Werner's syndrome, we noted heterozygosity for novel missense mutations in LMNA, specifically A57P, R133L (in two people), and L140R. 12927431

2003