Use of Targeted High-Throughput Sequencing for Genetic Classification of Patients with Bleeding Diathesis and Suspected Platelet Disorder

Inherited platelet disorders (IPD) form a rare and heterogeneous disease entity that is present in about 8% of patients with non-acquired bleeding diathesis. Identification of the defective cellular pathway is an important criterion for stratifying the patient's individual risk profile and for...

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Detalles Bibliográficos
Autores principales: Andres, Oliver, König, Eva-Maria, Althaus, Karina, Bakchoul, Tamam, Bugert, Peter, Eber, Stefan, Knöfler, Ralf, Kunstmann, Erdmute, Manukjan, Georgi, Meyer, Oliver, Strauß, Gabriele, Streif, Werner, Thiele, Thomas, Wiegering, Verena, Klopocki, Eva, Schulze, Harald
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Georg Thieme Verlag KG 2018
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6524924/
https://www.ncbi.nlm.nih.gov/pubmed/31249973
http://dx.doi.org/10.1055/s-0038-1676813

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6524924/
https://www.ncbi.nlm.nih.gov/pubmed/31249973
http://dx.doi.org/10.1055/s-0038-1676813

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