New Metabolic Phenotypes in Laminopathies:LMNAMutations in Patients with Severe Metabolic Syndrome-Reference-Cited by-同舟云学术

New Metabolic Phenotypes in Laminopathies:LMNAMutations in Patients with Severe Metabolic Syndrome

Published:2007-12-01 Issue:12 Volume:92 Page:4835-4844
ISSN:0021-972X
Container-title:The Journal of Clinical Endocrinology & Metabolism
language:en
Short-container-title:

Author:

Decaudain Aurélie¹²,Vantyghem Marie-Christine³,Guerci Bruno⁴,Hécart Annie-Claude⁵,Auclair Martine¹²,Reznik Yves⁶,Narbonne Hervé⁷,Ducluzeau Pierre-Henri⁸,Donadille Bruno¹²,Lebbé Céleste⁹,Béréziat Véronique¹²,Capeau Jacqueline¹⁰¹²,Lascols Olivier¹¹¹²,Vigouroux Corinne¹⁰¹²

Affiliation:

1. Université Pierre et Marie Curie-Paris6, Faculte de Médecine, UMR 5680 (A.D., M.A., B.D., V.B., J.C., O.L., C.V.), Paris, F-75012 France

2. INSERM U680 (A.D., M.A., B.D., V.B., J.C., O.L., C.V.), Paris, F-75012 France

3. Service d’Endocrinologie et Maladies Métaboliques (M.-C.V.), Centre Hospitalier Universitaire (CHU) de Lille, F-59037 France

4. Hôpital Jeanne d’Arc (B.G.), Service de Diabétologie, Endocrinologie et Nutrition, CHU Nancy, F-54201 France

5. Service d’Endocrinologie, Maladies Métaboliques et Médecine Interne (A.-C.H.), CHU de Reims, F-51092 France

6. Service d’Endocrinologie et Maladies Métaboliques (Y.R.), CHU Côte de Nacre, F-14033 France

7. Hôpital Sainte Marguerite, Assistance Publique-Hôpitaux de Marseille, Service de Nutrition, Maladies Métaboliques, Endocrinologie (H.N.), F-13274 Marseille, France

8. Centre de Recherche en Nutrition Humaine (P.-H.D.), Hospices Civils, Lyon, F-69002 France

9. AP-HP, Hôpital Saint-Louis (C.L.), Service de Dermatologie, Paris, F-75010 France

10. AP-HP, Hôpital Tenon, Service de Biochimie et d’Hormonologie (J.C., C.V.), Paris, F-75020 France

11. AP-HP, Hôpital Saint-Antoine, Département de Biologie Moléculaire (O.L.), F-75571 Paris, France

Publisher

The Endocrine Society

Subject

Biochemistry, medical,Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism

Link

http://academic.oup.com/jcem/article-pdf/92/12/4835/9054956/jcem4835.pdf

Reference42 articles.

1. Structural organization of the human gene encoding nuclear lamin A and nuclear lamin C.;Lin;J Biol Chem,1993

2. Nuclear lamins, diseases and aging.;Mattout;Curr Opin Cell Biol,2006

3. Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy.;Bonne;Nat Genet,1999

4. Identification of mutations in the gene encoding lamins A/C in autosomal dominant limb girdle muscular dystrophy with atrioventricular conduction disturbances (LGMD1B).;Muchir;Hum Mol Genet,2000

5. Missense mutations in the rod domain of the lamin A/C gene as causes of dilated cardiomyopathy and conduction-system disease.;Fatkin;N Engl J Med,1999

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