Your browser doesn't support javascript.
loading
Oculo-Cutaneous Albinism Type 4 (OCA4): Phenotype-Genotype Correlation.
Moreno-Artero, Ester; Morice-Picard, Fanny; Lasseaux, Eulalie; Robert, Matthieu P; Coste, Valentine; Michaud, Vincent; Leclerc-Mercier, Stéphanie; Bremond-Gignac, Dominique; Arveiler, Benoit; Hadj-Rabia, Smail.
Affiliation
  • Moreno-Artero E; Department of Dermatology, and Reference Centre for Genodermatoses and Rare Skin Diseases (MAGEC), Université Paris Descartes-Paris Cité, INSERM U1163, Institut Imagine, APHP, Hôpital Universitaire Necker-Enfants Malades, 75015 Paris, France.
  • Morice-Picard F; Department of Dermatology, Reference Centre for Genodermatoses and Rare Skin Diseases, INSERM U1312, Bordeaux University Hospital, 33000 Bordeaux, France.
  • Lasseaux E; Department of Medical Genetics, Bordeaux University Hospital, 33000 Bordeaux, France.
  • Robert MP; Department of Ophthalmology, and Reference Center for Rare Eye Diseases (OPHTARA), Université Paris Cité, Hôpital Universitaire Necker-Enfants Malades, APHP, 75015 Paris, France.
  • Coste V; Borelli Centre, UMR 9010, CNRS-SSA-ENS Paris Saclay-Université Paris Cité, 91190 Paris, France.
  • Michaud V; Department of Ophthalmology, Bordeaux University Hospital, 33000 Bordeaux, France.
  • Leclerc-Mercier S; Department of Medical Genetics, Bordeaux University Hospital, 33000 Bordeaux, France.
  • Bremond-Gignac D; INSERM U1211, Laboratory for Rare Diseases, Genetics and Metabolism, 33000 Bordeaux, France.
  • Arveiler B; Department of Pathology, and Reference Centre for Genodermatoses and Rare Skin Diseases (MAGEC), Université Paris Descartes-Paris Cité, APHP, Hôpital Universitaire Necker-Enfants Malades, 75015 Paris, France.
  • Hadj-Rabia S; Department of Ophthalmology, and Reference Center for Rare Eye Diseases (OPHTARA), Université Paris Cité, Hôpital Universitaire Necker-Enfants Malades, APHP, 75015 Paris, France.
Genes (Basel) ; 13(12)2022 11 23.
Article in En | MEDLINE | ID: mdl-36553465
Subject(s)
Key words
Fulltext
Add to My VHL
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Piebaldism Type of study: Prognostic_studies Limits: Humans Language: En Journal: Genes (Basel) Year: 2022 Document type: Article Affiliation country: Francia
Fulltext
Add to My VHL
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Piebaldism Type of study: Prognostic_studies Limits: Humans Language: En Journal: Genes (Basel) Year: 2022 Document type: Article Affiliation country: Francia