Lamin A Truncation in Hutchinson-Gilford Progeria-Reference-Cited by-同舟云学术

Lamin A Truncation in Hutchinson-Gilford Progeria

Published:2003-06-27 Issue:5628 Volume:300 Page:2055-2055
ISSN:0036-8075
Container-title:Science
language:en
Short-container-title:Science

Author:

De Sandre-Giovannoli Annachiara¹²³⁴⁵,Bernard Rafaëlle¹²³⁴⁵,Cau Pierre¹²³⁴⁵,Navarro Claire¹²³⁴⁵,Amiel Jeanne¹²³⁴⁵,Boccaccio Irène¹²³⁴⁵,Lyonnet Stanislas¹²³⁴⁵,Stewart Colin L.¹²³⁴⁵,Munnich Arnold¹²³⁴⁵,Le Merrer Martine¹²³⁴⁵,Lévy Nicolas¹²³⁴⁵

Affiliation:

1. Inserm U491: «Génétique Médicale et Développement», Faculté de Médecine Timone, Marseille, France.

2. Département de Génétique Médicale, Hôpital la Timone, Marseille, France.

3. Laboratoire de Biologie Cellulaire, Hôpital Conception, Marseille, France.

4. Inserm U393, Hôpital Necker, Paris, France.

5. Cancer and Developmental Biology Laboratory, NCI-Frederick, Frederick, MD 21702, USA.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

Reference6 articles.

1. Clinical and epidemiological information are available online at www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?cmd=entry&id=176670.

2. The nuclear lamina and inherited disease

3. Life at the edge: the nuclear envelope and human disease

4. Mandibuloacral Dysplasia Is Caused by a Mutation in LMNA-Encoding Lamin A/C

5. Materials and methods are available as supporting material on Science Online.

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