Cargando…
A novel mutation in SLC39A7 identified in a patient with autosomal recessive agammaglobulinemia: The impact of the J Project
| Autores principales: | , , , , , , , |
|---|---|
| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
John Wiley and Sons Inc.
2022
|
| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9327717/ https://www.ncbi.nlm.nih.gov/pubmed/35754127 http://dx.doi.org/10.1111/pai.13805 |
| _version_ | 1784757566004264960 |
|---|---|
| author | Erdős, Melinda Mironska, Kristina Kareva, Lidia Stavric, Katarina Hasani, Arijeta Lányi, Árpád Kállai, Judit Maródi, László |
| author_facet | Erdős, Melinda Mironska, Kristina Kareva, Lidia Stavric, Katarina Hasani, Arijeta Lányi, Árpád Kállai, Judit Maródi, László |
| author_sort | Erdős, Melinda |
| collection | PubMed |
| description | |
| format | Online Article Text |
| id | pubmed-9327717 |
| institution | National Center for Biotechnology Information |
| language | English |
| publishDate | 2022 |
| publisher | John Wiley and Sons Inc. |
| record_format | MEDLINE/PubMed |
| spelling | pubmed-93277172022-07-30 A novel mutation in SLC39A7 identified in a patient with autosomal recessive agammaglobulinemia: The impact of the J Project Erdős, Melinda Mironska, Kristina Kareva, Lidia Stavric, Katarina Hasani, Arijeta Lányi, Árpád Kállai, Judit Maródi, László Pediatr Allergy Immunol Clinical Letters John Wiley and Sons Inc. 2022-06-01 2022-06 /pmc/articles/PMC9327717/ /pubmed/35754127 http://dx.doi.org/10.1111/pai.13805 Text en © 2022 The Authors. Pediatric Allergy and Immunology published by European Academy of Allergy and Clinical Immunology and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
| spellingShingle | Clinical Letters Erdős, Melinda Mironska, Kristina Kareva, Lidia Stavric, Katarina Hasani, Arijeta Lányi, Árpád Kállai, Judit Maródi, László A novel mutation in SLC39A7 identified in a patient with autosomal recessive agammaglobulinemia: The impact of the J Project |
| title | A novel mutation in SLC39A7 identified in a patient with autosomal recessive agammaglobulinemia: The impact of the J Project |
| title_full | A novel mutation in SLC39A7 identified in a patient with autosomal recessive agammaglobulinemia: The impact of the J Project |
| title_fullStr | A novel mutation in SLC39A7 identified in a patient with autosomal recessive agammaglobulinemia: The impact of the J Project |
| title_full_unstemmed | A novel mutation in SLC39A7 identified in a patient with autosomal recessive agammaglobulinemia: The impact of the J Project |
| title_short | A novel mutation in SLC39A7 identified in a patient with autosomal recessive agammaglobulinemia: The impact of the J Project |
| title_sort | novel mutation in slc39a7 identified in a patient with autosomal recessive agammaglobulinemia: the impact of the j project |
| topic | Clinical Letters |
| url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9327717/ https://www.ncbi.nlm.nih.gov/pubmed/35754127 http://dx.doi.org/10.1111/pai.13805 |
| work_keys_str_mv | AT erdosmelinda anovelmutationinslc39a7identifiedinapatientwithautosomalrecessiveagammaglobulinemiatheimpactofthejproject AT mironskakristina anovelmutationinslc39a7identifiedinapatientwithautosomalrecessiveagammaglobulinemiatheimpactofthejproject AT karevalidia anovelmutationinslc39a7identifiedinapatientwithautosomalrecessiveagammaglobulinemiatheimpactofthejproject AT stavrickatarina anovelmutationinslc39a7identifiedinapatientwithautosomalrecessiveagammaglobulinemiatheimpactofthejproject AT hasaniarijeta anovelmutationinslc39a7identifiedinapatientwithautosomalrecessiveagammaglobulinemiatheimpactofthejproject AT lanyiarpad anovelmutationinslc39a7identifiedinapatientwithautosomalrecessiveagammaglobulinemiatheimpactofthejproject AT kallaijudit anovelmutationinslc39a7identifiedinapatientwithautosomalrecessiveagammaglobulinemiatheimpactofthejproject AT marodilaszlo anovelmutationinslc39a7identifiedinapatientwithautosomalrecessiveagammaglobulinemiatheimpactofthejproject AT erdosmelinda novelmutationinslc39a7identifiedinapatientwithautosomalrecessiveagammaglobulinemiatheimpactofthejproject AT mironskakristina novelmutationinslc39a7identifiedinapatientwithautosomalrecessiveagammaglobulinemiatheimpactofthejproject AT karevalidia novelmutationinslc39a7identifiedinapatientwithautosomalrecessiveagammaglobulinemiatheimpactofthejproject AT stavrickatarina novelmutationinslc39a7identifiedinapatientwithautosomalrecessiveagammaglobulinemiatheimpactofthejproject AT hasaniarijeta novelmutationinslc39a7identifiedinapatientwithautosomalrecessiveagammaglobulinemiatheimpactofthejproject AT lanyiarpad novelmutationinslc39a7identifiedinapatientwithautosomalrecessiveagammaglobulinemiatheimpactofthejproject AT kallaijudit novelmutationinslc39a7identifiedinapatientwithautosomalrecessiveagammaglobulinemiatheimpactofthejproject AT marodilaszlo novelmutationinslc39a7identifiedinapatientwithautosomalrecessiveagammaglobulinemiatheimpactofthejproject |