Cargando…
S178: A NEW HEREDITARY SYNDROME WITH SEVERE NEUTROPENIA AND NEUROLOGICAL INVOLVEMENT CAUSED BY THE AUTOSOMAL RECESSIVE COPZ1 MUTATION
| Autores principales: | , , , , , , , , , , , , |
|---|---|
| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Lippincott Williams & Wilkins
2023
|
| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10428277/ http://dx.doi.org/10.1097/01.HS9.0000967624.93623.49 |
| _version_ | 1785090429441540096 |
|---|---|
| author | Borbaran Bravo, Natalia Doll, Larissa Deordieva, Ekaterina Bräuning, Sandro Dannenmann, Benjamin Elgamacy, Mohammad Zakharova, Viktoria Lengerke, Claudia Zeidler, Cornelia Welte, Karl Shcherbina, Anna Skokowa, Julia Klimiankou, Maksim |
| author_facet | Borbaran Bravo, Natalia Doll, Larissa Deordieva, Ekaterina Bräuning, Sandro Dannenmann, Benjamin Elgamacy, Mohammad Zakharova, Viktoria Lengerke, Claudia Zeidler, Cornelia Welte, Karl Shcherbina, Anna Skokowa, Julia Klimiankou, Maksim |
| author_sort | Borbaran Bravo, Natalia |
| collection | PubMed |
| description | |
| format | Online Article Text |
| id | pubmed-10428277 |
| institution | National Center for Biotechnology Information |
| language | English |
| publishDate | 2023 |
| publisher | Lippincott Williams & Wilkins |
| record_format | MEDLINE/PubMed |
| spelling | pubmed-104282772023-08-17 S178: A NEW HEREDITARY SYNDROME WITH SEVERE NEUTROPENIA AND NEUROLOGICAL INVOLVEMENT CAUSED BY THE AUTOSOMAL RECESSIVE COPZ1 MUTATION Borbaran Bravo, Natalia Doll, Larissa Deordieva, Ekaterina Bräuning, Sandro Dannenmann, Benjamin Elgamacy, Mohammad Zakharova, Viktoria Lengerke, Claudia Zeidler, Cornelia Welte, Karl Shcherbina, Anna Skokowa, Julia Klimiankou, Maksim Hemasphere Oral Sessions Lippincott Williams & Wilkins 2023-08-08 /pmc/articles/PMC10428277/ http://dx.doi.org/10.1097/01.HS9.0000967624.93623.49 Text en Copyright © 2023 The Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access Abstract Book distributed under the Attribution-NonCommercial-NoDerivs (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) which allows third parties to download the articles and share them with others as long as they credit the author and the Abstract Book, but they cannot change the content in any way or use them commercially. |
| spellingShingle | Oral Sessions Borbaran Bravo, Natalia Doll, Larissa Deordieva, Ekaterina Bräuning, Sandro Dannenmann, Benjamin Elgamacy, Mohammad Zakharova, Viktoria Lengerke, Claudia Zeidler, Cornelia Welte, Karl Shcherbina, Anna Skokowa, Julia Klimiankou, Maksim S178: A NEW HEREDITARY SYNDROME WITH SEVERE NEUTROPENIA AND NEUROLOGICAL INVOLVEMENT CAUSED BY THE AUTOSOMAL RECESSIVE COPZ1 MUTATION |
| title | S178: A NEW HEREDITARY SYNDROME WITH SEVERE NEUTROPENIA AND NEUROLOGICAL INVOLVEMENT CAUSED BY THE AUTOSOMAL RECESSIVE COPZ1 MUTATION |
| title_full | S178: A NEW HEREDITARY SYNDROME WITH SEVERE NEUTROPENIA AND NEUROLOGICAL INVOLVEMENT CAUSED BY THE AUTOSOMAL RECESSIVE COPZ1 MUTATION |
| title_fullStr | S178: A NEW HEREDITARY SYNDROME WITH SEVERE NEUTROPENIA AND NEUROLOGICAL INVOLVEMENT CAUSED BY THE AUTOSOMAL RECESSIVE COPZ1 MUTATION |
| title_full_unstemmed | S178: A NEW HEREDITARY SYNDROME WITH SEVERE NEUTROPENIA AND NEUROLOGICAL INVOLVEMENT CAUSED BY THE AUTOSOMAL RECESSIVE COPZ1 MUTATION |
| title_short | S178: A NEW HEREDITARY SYNDROME WITH SEVERE NEUTROPENIA AND NEUROLOGICAL INVOLVEMENT CAUSED BY THE AUTOSOMAL RECESSIVE COPZ1 MUTATION |
| title_sort | s178: a new hereditary syndrome with severe neutropenia and neurological involvement caused by the autosomal recessive copz1 mutation |
| topic | Oral Sessions |
| url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10428277/ http://dx.doi.org/10.1097/01.HS9.0000967624.93623.49 |
| work_keys_str_mv | AT borbaranbravonatalia s178anewhereditarysyndromewithsevereneutropeniaandneurologicalinvolvementcausedbytheautosomalrecessivecopz1mutation AT dolllarissa s178anewhereditarysyndromewithsevereneutropeniaandneurologicalinvolvementcausedbytheautosomalrecessivecopz1mutation AT deordievaekaterina s178anewhereditarysyndromewithsevereneutropeniaandneurologicalinvolvementcausedbytheautosomalrecessivecopz1mutation AT brauningsandro s178anewhereditarysyndromewithsevereneutropeniaandneurologicalinvolvementcausedbytheautosomalrecessivecopz1mutation AT dannenmannbenjamin s178anewhereditarysyndromewithsevereneutropeniaandneurologicalinvolvementcausedbytheautosomalrecessivecopz1mutation AT elgamacymohammad s178anewhereditarysyndromewithsevereneutropeniaandneurologicalinvolvementcausedbytheautosomalrecessivecopz1mutation AT zakharovaviktoria s178anewhereditarysyndromewithsevereneutropeniaandneurologicalinvolvementcausedbytheautosomalrecessivecopz1mutation AT lengerkeclaudia s178anewhereditarysyndromewithsevereneutropeniaandneurologicalinvolvementcausedbytheautosomalrecessivecopz1mutation AT zeidlercornelia s178anewhereditarysyndromewithsevereneutropeniaandneurologicalinvolvementcausedbytheautosomalrecessivecopz1mutation AT weltekarl s178anewhereditarysyndromewithsevereneutropeniaandneurologicalinvolvementcausedbytheautosomalrecessivecopz1mutation AT shcherbinaanna s178anewhereditarysyndromewithsevereneutropeniaandneurologicalinvolvementcausedbytheautosomalrecessivecopz1mutation AT skokowajulia s178anewhereditarysyndromewithsevereneutropeniaandneurologicalinvolvementcausedbytheautosomalrecessivecopz1mutation AT klimiankoumaksim s178anewhereditarysyndromewithsevereneutropeniaandneurologicalinvolvementcausedbytheautosomalrecessivecopz1mutation |