A Novel LMNA Mutation Causes Altered Nuclear Morphology and Symptoms of Familial Partial Lipodystrophy (Dunnigan Variety) with Progeroid Features.
about
Familial partial lipodystrophy, Dunnigan variety - challenges for patient care during pregnancy: a case report.DNA damage accumulation and TRF2 degradation in atypical Werner syndrome fibroblasts with LMNA mutations.WRN Mutation Update: Mutation Spectrum, Patient Registries, and Translational Prospects[Werner syndrome. A prototypical form of segmental progeria.]Coronary artery disease in a Werner syndrome-like form of progeria characterized by low levels of progerin, a splice variant of lamin A.
P2860
A Novel LMNA Mutation Causes Altered Nuclear Morphology and Symptoms of Familial Partial Lipodystrophy (Dunnigan Variety) with Progeroid Features.
description
2010 nî lūn-bûn
@nan
2010 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
A Novel LMNA Mutation Causes A ...... iety) with Progeroid Features.
@ast
A Novel LMNA Mutation Causes A ...... iety) with Progeroid Features.
@en
A Novel LMNA Mutation Causes A ...... Familial Partial Lipodystrophy
@nl
type
label
A Novel LMNA Mutation Causes A ...... iety) with Progeroid Features.
@ast
A Novel LMNA Mutation Causes A ...... iety) with Progeroid Features.
@en
A Novel LMNA Mutation Causes A ...... Familial Partial Lipodystrophy
@nl
prefLabel
A Novel LMNA Mutation Causes A ...... iety) with Progeroid Features.
@ast
A Novel LMNA Mutation Causes A ...... iety) with Progeroid Features.
@en
A Novel LMNA Mutation Causes A ...... Familial Partial Lipodystrophy
@nl
P2093
P2860
P356
P1476
A Novel LMNA Mutation Causes A ...... riety) with Progeroid Features
@en
P2093
D F Leistritz
F M Hisama
G M Martin
K Friedrich
P2860
P304
P356
10.1159/000320166
P50
P577
2010-09-14T00:00:00Z