Overlapping syndrome with familial partial lipodystrophy, Dunnigan variety and cardiomyopathy due to amino-terminal heterozygous missense lamin A/C mutations
about
Overlapping syndromes in laminopathies: a meta-analysis of the reported literatureLMNA Sequences of 60,706 Unrelated Individuals Reveal 132 Novel Missense Variants in A-Type Lamins and Suggest a Link between Variant p.G602S and Type 2 DiabetesThe clinical approach to the detection of lipodystrophy - an AACE consensus statementA Novel LMNA Mutation Causes Altered Nuclear Morphology and Symptoms of Familial Partial Lipodystrophy (Dunnigan Variety) with Progeroid Features.Inner nuclear membrane proteins: impact on human disease.Lipodystrophy syndromesBarraquer-Simons syndrome: a rare form of acquired lipodystrophy.A woman with familial partial lipodystrophy and the complications of her four pregnancies.An Uncommon Association of Familial Partial Lipodystrophy, Dilated Cardiomyopathy, and Conduction System Disease.Genetic and clinical characteristics of skeletal and cardiac muscle in patients with lamin A/C gene mutations.Exploring the pathophysiology behind the more common genetic and acquired lipodystrophies.Lipodystrophies: adipose tissue disorders with severe metabolic implications.Spectrum of disease associated with partial lipodystrophy: lessons from a trial cohort.Lipodystrophic laminopathies: Diagnostic clues.
P2860
Q26851708-13EE2AAC-A602-4E00-8364-2A36D81413ACQ33799816-67853AC1-4A9F-4B5A-BDC4-1AEA58941E45Q33939518-FE958CFC-E86F-4988-ADA3-63B2BE4DDF61Q34215118-00A022C9-16F7-4D54-8C70-0660BB1A5AF0Q34252203-6EA84696-BC5F-4032-819F-36B9DAFABB7CQ34597209-765C3A04-BBC5-4015-BE58-37DF3D6019F4Q35961396-4457F946-D16F-495D-8866-F1FD15E86FE5Q37070351-9B2BD9B4-A2B6-49ED-972B-BA6276A8DC63Q37129185-B75FAB5E-17BA-41E0-A387-2E9C943FE870Q38085610-1BB5B71C-F74C-4312-8465-9965582EFFACQ38155007-ADCE88C8-B00D-42AF-B81C-A5BEB54A6A97Q38400624-956315E6-D02F-4F0F-98C3-357D4312D6D0Q47859313-CDC2652C-753D-4E43-BA60-9828D1407284Q51761347-C29AF2C8-1060-4428-919E-C9C4887D0D98
P2860
Overlapping syndrome with familial partial lipodystrophy, Dunnigan variety and cardiomyopathy due to amino-terminal heterozygous missense lamin A/C mutations
description
2009 nî lūn-bûn
@nan
2009 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
name
Overlapping syndrome with fami ...... s missense lamin A/C mutations
@ast
Overlapping syndrome with fami ...... s missense lamin A/C mutations
@en
type
label
Overlapping syndrome with fami ...... s missense lamin A/C mutations
@ast
Overlapping syndrome with fami ...... s missense lamin A/C mutations
@en
prefLabel
Overlapping syndrome with fami ...... s missense lamin A/C mutations
@ast
Overlapping syndrome with fami ...... s missense lamin A/C mutations
@en
P2093
P2860
P1433
P1476
Overlapping syndrome with fami ...... s missense lamin A/C mutations
@en
P2093
P2860
P356
10.1111/J.1399-0004.2009.01350.X
P577
2009-12-22T00:00:00Z