| Health / Medical Topics |
High Molecular Weight Kininogen Deficiency
A rare autosomal recessive inherited disorder characterized by prolonged partial thromboplastin time and absence of bleeding diathesis. (NCI Thesaurus)
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High mobility group protein HMG-I (107 aa, ~12 kDa) is encoded by the human HMGA1 gene. This protein plays a role in…
High mobility group protein B3 (200 aa, ~23 kDa) is encoded by the human HMGB3 gene. This protein is involved in DNA…
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