Matches in Nanopublications for { ?s ?p "[Mutations in KVLQT1 and KCNE1 also cause the Jervell and Lange-Nielsen syndrome, a form of LQTS associated with deafness, a phenotypic abnormality inherited in an autosomal recessive fashion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP160565.RABA9xQhSLGtvq0pS3p5Op3_6wZehuqTSTxA8P1fxc5qY130_assertion description "[Mutations in KVLQT1 and KCNE1 also cause the Jervell and Lange-Nielsen syndrome, a form of LQTS associated with deafness, a phenotypic abnormality inherited in an autosomal recessive fashion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP160565.RABA9xQhSLGtvq0pS3p5Op3_6wZehuqTSTxA8P1fxc5qY130_provenance.
- NP370153.RAwFqEZs75K3NMSFk97Vw8uOHUU6r3Qeoe4GVxsoyMvy0130_assertion description "[Mutations in KVLQT1 and KCNE1 also cause the Jervell and Lange-Nielsen syndrome, a form of LQTS associated with deafness, a phenotypic abnormality inherited in an autosomal recessive fashion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP370153.RAwFqEZs75K3NMSFk97Vw8uOHUU6r3Qeoe4GVxsoyMvy0130_provenance.
- NP374806.RA1xI7GDWza23M6X9E2AEQh5o_SZPl_ym5GFdwIpe9J-Q130_assertion description "[Mutations in KVLQT1 and KCNE1 also cause the Jervell and Lange-Nielsen syndrome, a form of LQTS associated with deafness, a phenotypic abnormality inherited in an autosomal recessive fashion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP374806.RA1xI7GDWza23M6X9E2AEQh5o_SZPl_ym5GFdwIpe9J-Q130_provenance.
- NP233356.RAgnqnpAZrse6M5RycVOCFFFopQYn5xY6egDr7F-6AR0Q130_assertion description "[Mutations in KVLQT1 and KCNE1 also cause the Jervell and Lange-Nielsen syndrome, a form of LQTS associated with deafness, a phenotypic abnormality inherited in an autosomal recessive fashion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP233356.RAgnqnpAZrse6M5RycVOCFFFopQYn5xY6egDr7F-6AR0Q130_provenance.
- NP479378.RA7rLcufNkEJKall2WEJWuiYX-S1qsP2PCoDXh-uUlO5U130_assertion description "[Mutations in KVLQT1 and KCNE1 also cause the Jervell and Lange-Nielsen syndrome, a form of LQTS associated with deafness, a phenotypic abnormality inherited in an autosomal recessive fashion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP479378.RA7rLcufNkEJKall2WEJWuiYX-S1qsP2PCoDXh-uUlO5U130_provenance.
- NP261345.RA74EYFF_gs56ufoeCrQ-zQDejlEYE3DJsRxCN7batJbw130_assertion description "[Mutations in KVLQT1 and KCNE1 also cause the Jervell and Lange-Nielsen syndrome, a form of LQTS associated with deafness, a phenotypic abnormality inherited in an autosomal recessive fashion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP261345.RA74EYFF_gs56ufoeCrQ-zQDejlEYE3DJsRxCN7batJbw130_provenance.
- assertion description "[Mutations in KVLQT1 and KCNE1 also cause the Jervell and Lange-Nielsen syndrome, a form of LQTS associated with deafness, a phenotypic abnormality inherited in an autosomal recessive fashion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP521584.RAE_wobPz0_U8kfABZYyXbwd6NijAYONXpKBs53ayonJE130_assertion description "[Mutations in KVLQT1 and KCNE1 also cause the Jervell and Lange-Nielsen syndrome, a form of LQTS associated with deafness, a phenotypic abnormality inherited in an autosomal recessive fashion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP521584.RAE_wobPz0_U8kfABZYyXbwd6NijAYONXpKBs53ayonJE130_provenance.
- NP294207.RA23R_09k4dG9KXB0hsyH2OqOXZ4khIKr_YrFqkC1m8ZI130_assertion description "[Mutations in KVLQT1 and KCNE1 also cause the Jervell and Lange-Nielsen syndrome, a form of LQTS associated with deafness, a phenotypic abnormality inherited in an autosomal recessive fashion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP294207.RA23R_09k4dG9KXB0hsyH2OqOXZ4khIKr_YrFqkC1m8ZI130_provenance.