Rett syndrome: a surprising result of mutation in MECP2. (Q34045865)
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(P1433) (Q2720965)
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(P1476) "Rett syndrome: a surprising result of mutation in MECP2." (language: en)
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(P2093) Dragich J
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Houwink-Manville I
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Schanen C
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(P2860) (Q24647294)
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(P854) https://opencitations.net/index/api/v1/citations/10.1073/PNAS.96.25.14412

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(P356) 10.1093/HMG/9.16.2365
(P698) 11005791