Učitavanje...

The molecular defect in type IIB von Willebrand disease. Identification of four potential missense mutations within the putative GpIb binding domain.

Type IIB von Willebrand Disease (vWD) is characterized by the selective loss of large von Willebrand Factor (vWF) multimers from plasma, presumably due to their increased reactivity with platelets and subsequent clearance from the circulation. Using the PCR, one of a panel of four potential missense...

Cijeli opis

Spremljeno u:
Bibliografski detalji
Glavni autori: Cooney, K A, Nichols, W C, Bruck, M E, Bahou, W F, Shapiro, A D, Bowie, E J, Gralnick, H R, Ginsburg, D
Format: Artigo
Jezik:Inglês
Izdano: 1991
Teme:
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC295141/
https://ncbi.nlm.nih.gov/pubmed/1672694
Oznake: Dodaj oznaku
Bez oznaka, Budi prvi tko označuje ovaj zapis!