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Investigation of troponin I mu...
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Investigation of troponin I mutations causing familial hypertrophic cardiomyopathy
Detalhes bibliográficos
Principais autores:
Abdulrazzak, H
,
Knott, A
,
Redwood, C
,
Esposito, G
,
Watkins, H
,
Marston, S
Formato:
Journal article
Publicado em:
2001
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