Hutchinson–Gilford Progeria Syndrome, Aging, and the Nuclear Lamina  

Oleh:

Korf, Bruce R.

Jenis: Article from Journal - ilmiah internasional
Dalam koleksi: The New England Journal of Medicine (keterangan: ada di Proquest) vol. 358 no. 06 (Feb. 2008), page 552.

Ketersediaan

Perpustakaan FK Nomor Panggil: N08.K.2008.01 Non-tandon: 1 (dapat dipinjam: 0) Tandon: tidak ada

Lihat Detail Induk

Isi artikel

We are living in a time that will probably be remembered as a golden age of discovery in human genetics. Most of the recent excitement has focused on the identification of genes that contribute to the risk of common diseases, so it is easy to forget how much can be learned from the study of rare "single-gene" disorders. Although barely noticed by most physicians, these rare disorders can impose an enormous burden on affected patients and their families. Characterization of the gene associated with a disorder provides the key to understanding the relevant pathophysiology, and this understanding may lead to . . .

Opini Anda

Klik untuk menuliskan opini Anda tentang koleksi ini!

Kembali