Matches in Nanopublications for { ?s ?p "[Mutations in the CDKL5 gene have been associated with the early-onset seizure variant of Rett syndrome and mutations in FOXG1 have been associated with the congenital Rett syndrome variant.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP198340.RArRBwglKeXj9ThUjl67qs00i9rEV_ugmUSjJbjw4hRn4130_assertion description "[Mutations in the CDKL5 gene have been associated with the early-onset seizure variant of Rett syndrome and mutations in FOXG1 have been associated with the congenital Rett syndrome variant.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP198340.RArRBwglKeXj9ThUjl67qs00i9rEV_ugmUSjJbjw4hRn4130_provenance.
- assertion description "[Mutations in the CDKL5 gene have been associated with the early-onset seizure variant of Rett syndrome and mutations in FOXG1 have been associated with the congenital Rett syndrome variant.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP925476.RAwnNrST5LxIJcp0fmv3H0rOKid87rd8XCGJCYI7oTexI130_assertion description "[Mutations in the CDKL5 gene have been associated with the early-onset seizure variant of Rett syndrome and mutations in FOXG1 have been associated with the congenital Rett syndrome variant.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP925476.RAwnNrST5LxIJcp0fmv3H0rOKid87rd8XCGJCYI7oTexI130_provenance.
- NP719319.RAZ0Qjgk6RCZm5LSX5cE3yCB0vX9yf6S4lvbAgQrVK5Rc130_assertion description "[Mutations in the CDKL5 gene have been associated with the early-onset seizure variant of Rett syndrome and mutations in FOXG1 have been associated with the congenital Rett syndrome variant.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP719319.RAZ0Qjgk6RCZm5LSX5cE3yCB0vX9yf6S4lvbAgQrVK5Rc130_provenance.
- assertion description "[Mutations in the CDKL5 gene have been associated with the early-onset seizure variant of Rett syndrome and mutations in FOXG1 have been associated with the congenital Rett syndrome variant.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Mutations in the CDKL5 gene have been associated with the early-onset seizure variant of Rett syndrome and mutations in FOXG1 have been associated with the congenital Rett syndrome variant.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1012164.RACyjnFhIAbv78GCJYGoHypQZhoO7QAfaR9mD7z_wj6WI130_assertion description "[Mutations in the CDKL5 gene have been associated with the early-onset seizure variant of Rett syndrome and mutations in FOXG1 have been associated with the congenital Rett syndrome variant.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1012164.RACyjnFhIAbv78GCJYGoHypQZhoO7QAfaR9mD7z_wj6WI130_provenance.
- NP1012165.RAr6MICdEX_02N3Bh7Sf5BpMO3r_um3arhluDPwTBsTxg130_assertion description "[Mutations in the CDKL5 gene have been associated with the early-onset seizure variant of Rett syndrome and mutations in FOXG1 have been associated with the congenital Rett syndrome variant.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1012165.RAr6MICdEX_02N3Bh7Sf5BpMO3r_um3arhluDPwTBsTxg130_provenance.
- NP404333.RAwd34ngQfY2IIWQpar9Qt4svIdEzxatxELphuOnlXVk8130_assertion description "[Mutations in the CDKL5 gene have been associated with the early-onset seizure variant of Rett syndrome and mutations in FOXG1 have been associated with the congenital Rett syndrome variant.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP404333.RAwd34ngQfY2IIWQpar9Qt4svIdEzxatxELphuOnlXVk8130_provenance.
- NP719308.RAPErmbtxrtd6KCDyplJaa1sVyLXpKxBLOO4fwJ5OIxtE130_assertion description "[Mutations in the CDKL5 gene have been associated with the early-onset seizure variant of Rett syndrome and mutations in FOXG1 have been associated with the congenital Rett syndrome variant.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP719308.RAPErmbtxrtd6KCDyplJaa1sVyLXpKxBLOO4fwJ5OIxtE130_provenance.
- NP1012159.RANU7LGc2byL-JXs0KFgalPTON-K-tBu5GxNW6qj1lcbE130_assertion description "[Mutations in the CDKL5 gene have been associated with the early-onset seizure variant of Rett syndrome and mutations in FOXG1 have been associated with the congenital Rett syndrome variant.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1012159.RANU7LGc2byL-JXs0KFgalPTON-K-tBu5GxNW6qj1lcbE130_provenance.