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A Three-generation Family Presenting Five Cases of Homozygosity for the 20210 G to A Prothrombin Variant
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1998
Year
Allelic VariantMendelian DisorderGenetic DisorderGeneticsInherited Metabolic DiseaseGenetic EpidemiologyMolecular BiologyA Prothrombin VariantMolecular GeneticsGenetic VariationMedical GeneticsChromosomal RearrangementMedicineGenetic MedicineVariant InterpretationClinical Genetics
A Three-generation Family Presenting Five Cases of Homozygosity for the 20210 G to A Prothrombin Variant -