Hereditary Thrombotic Thrombocytopenic Purpura

Hereditary thrombotic thrombocytopenic purpura (hTTP), also known as Upshaw–Schulman syndrome, is a rare genetic disorder caused by mutations in the ADAMTS13 gene that leads to decreased or absent production of the plasma von Willebrand factor (VWF)-cleaving metalloprotease ADAMTS13. The result is c...

Descripción completa

Detalles Bibliográficos
Autores principales: Nusrat, Sanober, Beg, Kisha, Khan, Osman, Sinha, Arpan, George, James
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10606562/
https://www.ncbi.nlm.nih.gov/pubmed/37895305
http://dx.doi.org/10.3390/genes14101956

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10606562/
https://www.ncbi.nlm.nih.gov/pubmed/37895305
http://dx.doi.org/10.3390/genes14101956

Ejemplares similares