MECP2 mutations in sporadic cases of Rett syndrome are almost exclusively of paternal origin (Q24533455)
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Current Data About MECP2 mutations in sporadic cases of Rett syndrome are almost exclusively of paternal origin
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(P1932) R Trappe

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(P1476) "MECP2 mutations in sporadic cases of Rett syndrome are almost exclusively of paternal origin" (language: en)

(P2093) F Laccone
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J Cobilanschi
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M Meins
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P Huppke
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F Hanefeld
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W Engel
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(P854) https://pubmed.ncbi.nlm.nih.gov/11309679
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External Links
(P356) 10.1086/320109
(P698) 11309679
(P932) 1226090
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