Publication | Closed Access
A rapid automated SSCP multiplex capillary electrophoresis protocol that detects the two common mutations implicated in hereditary hemochromatosis (HH)
30
Citations
14
References
1999
Year
Hereditary HemochromatosisGenetic DisorderMedicineGeneticsPathologyLaboratory MedicineMolecular GeneticsCommon MutationsDisease Gene IdentificationMolecular Diagnostics
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