Cargando…
Glanzmann Thrombasthenia in Pakistani Patients: Identification of 7 Novel Pathogenic Variants in the Fibrinogen Receptor αIIbβ3
Glanzmann thrombasthenia (GT) is a rare autosomal recessive inherited platelet disorder occurring frequently in populations with high incidence of consanguineous marriages. GT is characterized by quantitative and/or qualitative defect of the platelet αIIbβ3 (GPIIb/IIIa) receptor caused by pathogenic...
Autores principales: | Siddiqi, Muhammad Younus Jamal, Boeckelmann, Doris, Naz, Arshi, Imran, Ayisha, Ahmed, Shariq, Najmuddin, Akbar, Zieger, Barbara |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9856889/ https://www.ncbi.nlm.nih.gov/pubmed/36672149 http://dx.doi.org/10.3390/cells12020213 |
Ejemplares similares
-
Glanzmann thrombasthenia
por: Nurden, Alan T
Publicado: (2006) -
Glanzmann’s thrombasthenia and molecular mimicry
por: Wiwanitkit, Viroj
Publicado: (2010) -
Disease Burden in Patients with Glanzmann’s Thrombasthenia: Perspectives from the Glanzmann’s Thrombasthenia Patient/Caregiver Questionnaire
por: Duncan, Alexander, et al.
Publicado: (2020) -
The Glanzmann Thrombasthenia Registry: safety of platelet therapy in patients with Glanzmann thrombasthenia and changes in alloimmunization status
por: Poon, Man-Chiu, et al.
Publicado: (2023) -
Dental Considerations in the Management of Glanzmann’s Thrombasthenia
por: Mehta, Diana N, et al.
Publicado: (2010)