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Titre
Mutations in DDHD1, encoding a phospholipase A1, is a novel cause of retinopathy and neurodegeneration with brain iron accumulation
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BSO - Titre
Mutations in DDHD1 , encoding a phospholipase A1, is a novel cause of retinopathy and neurodegeneration with brain iron accumulation
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DOI
DOI
10.1016/j.ejmg.2017.08.015
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DOAI
DOAI
10.1016/j.ejmg.2017.08.015
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Identifiant WoS
WOS:000417205900004
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Accès ouvert
OA - Non
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Source - Accès ouvert
OA - Non
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Type d'accès
Non OA
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Editeur
Elsevier
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Source
EUROPEAN JOURNAL OF MEDICAL GENETICS
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ISSN
1769-7212
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Type de document
Article
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Notoriété
2 - Acceptable
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CNRS
Oui
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CNRS - Institut
INSB - Institut des sciences biologiques
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uid:/52RTRQ4B
12/10/2021 14:52:58 (latest)
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