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F1000 Research Ltd
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Case report: investigation and molecular genetic diagnosis of familial hypomagnesaemia.
Willows, Jamie.
F1000 Research Ltd.
2019-01-01
Case report: investigation and molecular genetic diagnosis of familial hypomagnesaemia.
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Arrhythmias, Cardiac--Oman
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Molecular genetics--Oman
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Willows, Jamie.
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sfy39587stp18
