A syndrome combining severe hypotrichosis and macular dystrophy: absence of mutations in TIMP genes

Autor:	Nadia Raison-Peyron, L. Durand, P.A. Duval, B. Arnaud, C. Hamel, G. Barneon, J. Meynadier
Rok vydání:	2000
Předmět:	Genetics Mutation Pathology medicine.medical_specialty Eye disease Dystrophy Dermatology Macular dystrophy Biology medicine.disease medicine.disease_cause medicine Hypotrichosis Gene Retinopathy Severe hypotrichosis
Zdroj:	British Journal of Dermatology. 143:902-904
ISSN:	0007-0963
DOI:	10.1046/j.1365-2133.2000.03803.x
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::fc2676a61b9de10f83dc95db20d0867a https://doi.org/10.1046/j.1365-2133.2000.03803.x Zobrazit plný text záznamu Plný text