Publication | Open Access
Germline Heterozygous Variants in SEC23B Are Associated with Cowden Syndrome and Enriched in Apparently Sporadic Thyroid Cancer
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Citations
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References
2015
Year
Somatic VariantGenetic DisorderGeneticsThyroid DiseasePathologyCowden SyndromeMolecular GeneticsGenomicsMedicineGermline Heterozygous VariantsSec23b Are AssociatedVariant InterpretationClinical Genetics
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