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. 2005 Feb;42(2):e15. doi: 10.1136/jmg.2004.026161
Mutations in exon 1 of MECP2 are a rare cause of Rett syndrome
R Amir
, P Fang
, Z Yu
, D Glaze
, A Percy
, H Zoghbi
, B Roa
, I B Van den Veyver
R Amir
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P Fang
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Z Yu
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D Glaze
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A Percy
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H Zoghbi
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B Roa
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I B Van den Veyver
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PMCID: PMC1735975 PMID: 15689438