Work

Coats' Plus: A Progressive Familial Syndrome of Bilateral Coats' Disease, Characteristic Cerebral Calcification, Leukoencephalopathy, Slow Pre- and Post-Natal Linear Growth and Defects of Bone Marrow and Integument

Year: 2004

Type: article

Study design: Case Report

Source: Neuropediatrics

DOI: 10.1055/s-2003-43552

Authors: Y. Crow, J. McMenamin, C. Haenggeli, D. Hadley, S. Tirupathi, E. Treacy, S. Zuberi, B. Browne, J. Tolmie, J. Stephenson

Institutions: University of Leeds, St James's University Hospital, Children's Health Ireland at Crumlin, University Hospital of Geneva, Southern General Hospital, Temple Street Children's University Hospital, Royal Hospital for Children, Glasgow Royal Infirmary

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: W181405868

FWCI: 1.245

Cites:

Cited by: 89

Related to: 10