Matches in Nanopublications for { ?s ?p "[Following the recent discovery that the methyl-CpG binding protein 2 (MECP2) gene located on Xq28 is involved in Rett syndrome (RTT), a wild spectrum of phenotypes, including mental handicap, has been shown to be associated with mutations in MECP2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP912095.RA91Twor7aZNzm2BUkqOZvOpTyfp0QFpnomoAez6tMTSo130_assertion description "[Following the recent discovery that the methyl-CpG binding protein 2 (MECP2) gene located on Xq28 is involved in Rett syndrome (RTT), a wild spectrum of phenotypes, including mental handicap, has been shown to be associated with mutations in MECP2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP912095.RA91Twor7aZNzm2BUkqOZvOpTyfp0QFpnomoAez6tMTSo130_provenance.
- assertion description "[Following the recent discovery that the methyl-CpG binding protein 2 (MECP2) gene located on Xq28 is involved in Rett syndrome (RTT), a wild spectrum of phenotypes, including mental handicap, has been shown to be associated with mutations in MECP2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP314932.RA2ju4jnmDuavWCoH2OiS_ePz0mkdzTZLNW-MrCsogZ2k130_assertion description "[Following the recent discovery that the methyl-CpG binding protein 2 (MECP2) gene located on Xq28 is involved in Rett syndrome (RTT), a wild spectrum of phenotypes, including mental handicap, has been shown to be associated with mutations in MECP2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP314932.RA2ju4jnmDuavWCoH2OiS_ePz0mkdzTZLNW-MrCsogZ2k130_provenance.