Mandibuloacral dysplasia type A in childhood-Reference-Cited by-同舟云学术

Mandibuloacral dysplasia type A in childhood

Published:2009-10 Issue:10 Volume:149A Page:2258-2264
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Garavelli L.,D'Apice M.R.,Rivieri F.,Bertoli M.,Wischmeijer A.,Gelmini C.,De Nigris V.,Albertini E.,Rosato S.,Virdis R.,Bacchini E.,Dal Zotto R.,Banchini G.,Iughetti L.,Bernasconi S.,Superti-Furga A.,Novelli G.

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference21 articles.

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2. Severe mandibuloacral dysplasia associated lipodystrophy and progeria in a young girl with a novel homozygous Arg527Cys LMNA mutation;Agarwal;J Clin Endocrinol Metab,2008

3. Nuclear lamins: Laminopathies and their role in premature ageing;Broers;Physiol Rev,2006

4. The laminopathies: The functional architecture of the nucleus and its contribution to disease;Burke;Annu Rev Genomics Hum Genet,2006

5. LMNA is mutated in Hutchinson-Gilford progeria (MIM 176670) but not in Wiedemann-Rautenstrauch progeroid syndrome (MIM 264090);Cao;J Hum Genet,2003

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