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Two novel mutations in SLC6A8 cause creatine transporter defect and distinctive X-linked mental retardation in two unrelated dutch families
Authors
Femke Aarsen
Coriene Catsman - Berrevoets
+8Â more
IFM Coo
M (Mercedes) Duran
Jan Huijmans
C Jakobs
Jozef Kamphoven
GS Salomons
MS van der Knaap
Grazia Verheijen - Mancini
Publication date
1 January 2005
Publisher
Abstract
Abstract is not available.
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Last time updated on 29/05/2023
