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dc.rights.licenseopenen_US
dc.contributor.authorBATAILLE, Pauline
dc.contributor.authorMICHAUD, Vincent
IDREF: 243713878
dc.contributor.authorROBERT, Matthieu P
dc.contributor.authorBEKEL, Lilia
dc.contributor.authorLECLERC-MERCIER, Stéphanie
dc.contributor.authorHARROCHE, Annie
dc.contributor.authorCELERIER, Charlotte
dc.contributor.authorLASSEAUX, Eulalie
dc.contributor.authorBORGEL, Delphine
dc.contributor.authorBREMOND-GIGNAC, Dominique
dc.contributor.authorBODEMER, Christine
hal.structure.identifierLaboratoire Maladies Rares: Génétique et Métabolisme (Bordeaux) [U1211 INSERM/MRGM]
dc.contributor.authorARVEILER, Benoit
dc.contributor.authorHADJ-RABIA, Smaïl
dc.date.accessioned2022-11-29T16:42:16Z
dc.date.available2022-11-29T16:42:16Z
dc.date.issued2020-03-01
dc.identifier.issn1399-0004en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/170424
dc.language.isoENen_US
dc.subject.enAlbinism
dc.subject.enOculocutaneous
dc.subject.enChild
dc.subject.enFemale
dc.subject.enFounder Effect
dc.subject.enGenetic Predisposition to Disease
dc.subject.enHumans
dc.subject.enMembrane Proteins
dc.subject.enPedigree
dc.subject.enReceptors
dc.subject.enLDL
dc.title.enClinical variability and probable founder effect in oculocutaneous albinism type 7.
dc.title.alternativeClin Geneten_US
dc.typeArticle de revueen_US
dc.identifier.doi10.1111/cge.13655en_US
dc.subject.halSciences du Vivant [q-bio]/Médecine humaine et pathologieen_US
dc.identifier.pubmed31694064en_US
bordeaux.journalClinical Geneticsen_US
bordeaux.page527-528en_US
bordeaux.volume97en_US
bordeaux.hal.laboratoriesMaladies Rares : Génétique et Métabolisme (MRGM) - UMR 1211en_US
bordeaux.issue3en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionINSERMen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
bordeaux.import.sourcepubmed
hal.identifierhal-03878371
hal.version1
hal.date.transferred2022-11-29T16:42:21Z
hal.exporttrue
workflow.import.sourcepubmed
dc.rights.ccPas de Licence CCen_US
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