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Functional characterisation of point mutations in cardiac troponin I that cause familial hypertrophic cardiomyopathy

No description available.
Identiferoai:union.ndltd.org:bl.uk/oai:ethos.bl.uk:393455
Date January 2001
CreatorsElliott, Kathryn
PublisherUniversity of Oxford
Source SetsEthos UK
Detected LanguageEnglish
TypeElectronic Thesis or Dissertation

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