ITEM METADATA RECORD
Title: Mutations in exon 1 of MECP2B are not a common cause of X-linked mental retardation in males
Authors: Poirier, K ×
Francis, F
Hamel, B
Moraine, C
Fryns, Jean-Pierre
Ropers, HH
Chelly, J
Bienvenu, T #
Issue Date: May-2005
Publisher: Karger
Series Title: European Journal of Human Genetics vol:13 issue:5 pages:523-524
ISSN: 1018-4813
Publication status: published
KU Leuven publication type: IT
Appears in Collections:Clinical Genetics Section (-)
Department of Human Genetics - miscellaneous
× corresponding author
# (joint) last author

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