Neonatal progeria: increased ratio of progerin to lamin A leads to progeria of the newborn

Author:

Reunert Janine,Wentzell Rüdiger,Walter Michael,Jakubiczka Sibylle,Zenker Martin,Brune Thomas,Rust Stephan,Marquardt Thorsten

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Reference32 articles.

1. Gilford H : Progeria: a form of senilism. Practitioner 1904; 73: 188–217.

2. Hutchinson J : Congenital absence of hair and mammary glands with atrophic condition of the skin and its appendages in a boy whose mother had been almost totally bald from alopecia areata from the age of six. Med Chirurg Trans 1886; 69: 36.

3. De Sandre-Giovannoli A, Bernard R, Cau P et al: Lamin A truncation in Hutchinson-Gilford progeria. Science 2003; 300: 2055.

4. Eriksson M, Brown WT, Gordon LB et al: Recurrent de novo point mutations in lamin A cause Hutchinson-Gilford progeria syndrome. Nature 2003; 423: 293–298.

5. Pendás AM, Zhou Z, Cadiñanos J et al: Defective prelamin A processing and muscular and adipocyte alterations in Zmpste24 metalloproteinase-deficient mice. Nat Genet 2002; 31: 94–99.

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