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- Q59578328 description "dissertation" @default.
- Q59578328 description "doctoral thesis by Kathryn Elliott" @default.
- Q59578328 description "doctoral thesis by Kathryn Elliott" @default.
- Q59578328 description "doctoral thesis by Kathryn Elliott" @default.
- Q59578328 description "proefschrift" @default.
- Q59578328 description "tesis doctoral" @default.
- Q59578328 description "thèse de doctorat" @default.
- Q59578328 description "traethawd ymchwil" @default.
- Q59578328 description "дисертація" @default.
- Q59578328 name "Functional characterisation of point mutations in cardiac troponin I that cause familial hypertrophic cardiomyopathy" @default.
- Q59578328 name "Functional characterisation of point mutations in cardiac troponin I that cause familial hypertrophic cardiomyopathy" @default.
- Q59578328 name "Functional characterisation of point mutations in cardiac troponin I that cause familial hypertrophic cardiomyopathy" @default.
- Q59578328 name "Functional characterisation of point mutations in cardiac troponin I that cause familial hypertrophic cardiomyopathy" @default.
- Q59578328 name "Functional characterisation of point mutations in cardiac troponin I that cause familial hypertrophic cardiomyopathy" @default.
- Q59578328 name "Functional characterisation of point mutations in cardiac troponin I that cause familial hypertrophic cardiomyopathy" @default.
- Q59578328 name "Functional characterisation of point mutations in cardiac troponin I that cause familial hypertrophic cardiomyopathy" @default.
- Q59578328 name "Functional characterisation of point mutations in cardiac troponin I that cause familial hypertrophic cardiomyopathy" @default.
- Q59578328 type Item @default.
- Q59578328 label "Functional characterisation of point mutations in cardiac troponin I that cause familial hypertrophic cardiomyopathy" @default.
- Q59578328 label "Functional characterisation of point mutations in cardiac troponin I that cause familial hypertrophic cardiomyopathy" @default.
- Q59578328 label "Functional characterisation of point mutations in cardiac troponin I that cause familial hypertrophic cardiomyopathy" @default.
- Q59578328 label "Functional characterisation of point mutations in cardiac troponin I that cause familial hypertrophic cardiomyopathy" @default.
- Q59578328 label "Functional characterisation of point mutations in cardiac troponin I that cause familial hypertrophic cardiomyopathy" @default.
- Q59578328 label "Functional characterisation of point mutations in cardiac troponin I that cause familial hypertrophic cardiomyopathy" @default.
- Q59578328 label "Functional characterisation of point mutations in cardiac troponin I that cause familial hypertrophic cardiomyopathy" @default.
- Q59578328 label "Functional characterisation of point mutations in cardiac troponin I that cause familial hypertrophic cardiomyopathy" @default.
- Q59578328 prefLabel "Functional characterisation of point mutations in cardiac troponin I that cause familial hypertrophic cardiomyopathy" @default.
- Q59578328 prefLabel "Functional characterisation of point mutations in cardiac troponin I that cause familial hypertrophic cardiomyopathy" @default.
- Q59578328 prefLabel "Functional characterisation of point mutations in cardiac troponin I that cause familial hypertrophic cardiomyopathy" @default.
- Q59578328 prefLabel "Functional characterisation of point mutations in cardiac troponin I that cause familial hypertrophic cardiomyopathy" @default.
- Q59578328 prefLabel "Functional characterisation of point mutations in cardiac troponin I that cause familial hypertrophic cardiomyopathy" @default.
- Q59578328 prefLabel "Functional characterisation of point mutations in cardiac troponin I that cause familial hypertrophic cardiomyopathy" @default.
- Q59578328 prefLabel "Functional characterisation of point mutations in cardiac troponin I that cause familial hypertrophic cardiomyopathy" @default.
- Q59578328 prefLabel "Functional characterisation of point mutations in cardiac troponin I that cause familial hypertrophic cardiomyopathy" @default.
- Q59578328 P1476 Q59578328-244CFB27-4791-4B9D-AE73-38B2258C59B8 @default.
- Q59578328 P2093 Q59578328-70067158-A462-454D-B0AE-4BFC1252C6D5 @default.
- Q59578328 P31 Q59578328-D514A394-3830-40FE-B2B5-E6A5D9B7FC7C @default.
- Q59578328 P4101 Q59578328-E8025EFC-A1C5-4F95-81EB-41630FC7E4EE @default.
- Q59578328 P4536 Q59578328-B12B45B5-E186-45B2-B551-5ACB2890714B @default.
- Q59578328 P577 Q59578328-A606BB23-A3C0-4B28-ACE5-BD7B471875A3 @default.
- Q59578328 P1476 "Functional characterisation of point mutations in cardiac troponin I that cause familial hypertrophic cardiomyopathy" @default.
- Q59578328 P2093 "Kathryn Elliott" @default.
- Q59578328 P31 Q187685 @default.
- Q59578328 P4101 Q34433 @default.
- Q59578328 P4536 "uk.bl.ethos.393455" @default.
- Q59578328 P577 "2001-01-01T00:00:00Z" @default.