Work

Hutchinson-Gilford syndrome (progeria)

Year: 2009

Type: article

Abstract: Progeria is a rare, autosomal dominant, progeroid disorder. In the world literature less than 100 cases have been reported to date. We present this case because of its rarity.

Source: Indian Journal of Dermatology

DOI: 10.4103/0019-5154.45438

Authors: Amar Surjushe, Minal Thakre, Resham Vasani, Dattatray Saple

Institution: Grant Medical College and Sir Jamshedjee Jeejeebhoy Group of Hospitals

Language: English

Topic: Nuclear Structure and Function

Subfield: Molecular Biology

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: diamond

OpenAlex ID: W2015312949

FWCI: 0.327

Cites:

Cited by: 5

Related to: 10