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Mutation detection and inhibitor risk in Iranian patients with Hemophilia A: Six novel mutations
This investigation facilitates a better understanding of inhibitor development, the critical treatment morbidity in HA patients. Furthermore, six novel mutations are reported, which would expand the mutation spectrum of the F8 gene.
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7752620/ https://www.ncbi.nlm.nih.gov/pubmed/33363863 http://dx.doi.org/10.1002/ccr3.3294 |
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author | Nasirnejad Sola, Farzaneh Morovvati, Saeid Sabetghadam Moghadam, Mitra Entezari, Malihe |
author_facet | Nasirnejad Sola, Farzaneh Morovvati, Saeid Sabetghadam Moghadam, Mitra Entezari, Malihe |
author_sort | Nasirnejad Sola, Farzaneh |
collection | PubMed |
description | This investigation facilitates a better understanding of inhibitor development, the critical treatment morbidity in HA patients. Furthermore, six novel mutations are reported, which would expand the mutation spectrum of the F8 gene. |
format | Online Article Text |
id | pubmed-7752620 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-77526202020-12-23 Mutation detection and inhibitor risk in Iranian patients with Hemophilia A: Six novel mutations Nasirnejad Sola, Farzaneh Morovvati, Saeid Sabetghadam Moghadam, Mitra Entezari, Malihe Clin Case Rep Case Reports This investigation facilitates a better understanding of inhibitor development, the critical treatment morbidity in HA patients. Furthermore, six novel mutations are reported, which would expand the mutation spectrum of the F8 gene. John Wiley and Sons Inc. 2020-09-15 /pmc/articles/PMC7752620/ /pubmed/33363863 http://dx.doi.org/10.1002/ccr3.3294 Text en © 2020 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Reports Nasirnejad Sola, Farzaneh Morovvati, Saeid Sabetghadam Moghadam, Mitra Entezari, Malihe Mutation detection and inhibitor risk in Iranian patients with Hemophilia A: Six novel mutations |
title | Mutation detection and inhibitor risk in Iranian patients with Hemophilia A: Six novel mutations |
title_full | Mutation detection and inhibitor risk in Iranian patients with Hemophilia A: Six novel mutations |
title_fullStr | Mutation detection and inhibitor risk in Iranian patients with Hemophilia A: Six novel mutations |
title_full_unstemmed | Mutation detection and inhibitor risk in Iranian patients with Hemophilia A: Six novel mutations |
title_short | Mutation detection and inhibitor risk in Iranian patients with Hemophilia A: Six novel mutations |
title_sort | mutation detection and inhibitor risk in iranian patients with hemophilia a: six novel mutations |
topic | Case Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7752620/ https://www.ncbi.nlm.nih.gov/pubmed/33363863 http://dx.doi.org/10.1002/ccr3.3294 |
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