Publication | Open Access
Ten candidate ADAMTS13 mutations in six French families with congenital thrombotic thrombocytopenic purpura (Upshaw–Schulman syndrome)
113
Citations
23
References
2004
Year
French FamiliesGenetic DisorderGeneticsGenetic EpidemiologyCandidate Adamts13 MutationsPathologyMedical GeneticsUpshaw–schulman SyndromeDisease Gene IdentificationMedicineClinical Genetics
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