Work

An Atypical Presentation of Dyskeratosis Congenita in a Child With a Familial RTEL1 Mutation

Year: 2024

Type: article

Study design: Case Report

Source: Pediatric Dermatology

DOI: 10.1111/pde.15750

Authors: Faiza Ahmed, Kristina Blegen, Michelle Tarbox

Institution: Texas Tech University Health Sciences Center

Language: English

Topic: Genetic and rare skin diseases.

Subfield: Genetics

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

OpenAlex ID: W4402654182

FWCI: 0.24

Cites: 22

Cited by: 1

Related to: 10