(Q48640742)
Statements
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MECP2 mutation in a boy with severe neonatal encephalopathy: clinical, neuropathological and molecular findings (English)
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Gabreëls FJ
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Geerdink N
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Rotteveel JJ
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Lammens M
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Sistermans EA
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Heikens GT
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Mullaart RA
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Hamel BC
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1 February 2002
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33
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1
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33-36
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Identifiers
1 reference