Clinical Features and Gene Mutation Analysis of Congenital Thrombotic Thrombocytopenic Purpura in Neonates

Congenital thrombotic thrombocytopenic purpura (TTP) is a rare hereditary disease with a high mortality rate; however, improved patient survival is possible with prompt diagnosis and treatment. The clinical features and mutation sites of a disintegrin and metalloproteinase with thrombospondin motifs...

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Detalles Bibliográficos
Autores principales: Wang, Jiali, Zhao, Li
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Pediatrics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7536282/
https://www.ncbi.nlm.nih.gov/pubmed/33072671
http://dx.doi.org/10.3389/fped.2020.546248

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7536282/
https://www.ncbi.nlm.nih.gov/pubmed/33072671
http://dx.doi.org/10.3389/fped.2020.546248

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