Concomitant constitutive LNK and NFE2 mutation with loss of sumoylation in a case of hereditary thrombocythemia

Detalles Bibliográficos
Autores principales: Böckelmann, Lukas Clemens, Basu, Titiksha, Gründer, Albert, Wang, Wei, Breucker, Jan, Kaiser, Sandra, Pichler, Andrea, Pahl, Heike Luise
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Fondazione Ferrata Storti 2021
Materias:
Letters to the Editor
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8018143/
https://www.ncbi.nlm.nih.gov/pubmed/32554556
http://dx.doi.org/10.3324/haematol.2020.246587
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author Böckelmann, Lukas Clemens
Basu, Titiksha
Gründer, Albert
Wang, Wei
Breucker, Jan
Kaiser, Sandra
Pichler, Andrea
Pahl, Heike Luise
author_facet Böckelmann, Lukas Clemens
Basu, Titiksha
Gründer, Albert
Wang, Wei
Breucker, Jan
Kaiser, Sandra
Pichler, Andrea
Pahl, Heike Luise
author_sort Böckelmann, Lukas Clemens
collection PubMed
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spelling pubmed-80181432021-04-05 Concomitant constitutive LNK and NFE2 mutation with loss of sumoylation in a case of hereditary thrombocythemia Böckelmann, Lukas Clemens Basu, Titiksha Gründer, Albert Wang, Wei Breucker, Jan Kaiser, Sandra Pichler, Andrea Pahl, Heike Luise Haematologica Letters to the Editor Fondazione Ferrata Storti 2021-04-01 /pmc/articles/PMC8018143/ /pubmed/32554556 http://dx.doi.org/10.3324/haematol.2020.246587 Text en Copyright© 2021 Ferrata Storti Foundation http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Noncommercial License (by-nc 4.0) which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
spellingShingle Letters to the Editor
Böckelmann, Lukas Clemens
Basu, Titiksha
Gründer, Albert
Wang, Wei
Breucker, Jan
Kaiser, Sandra
Pichler, Andrea
Pahl, Heike Luise
Concomitant constitutive LNK and NFE2 mutation with loss of sumoylation in a case of hereditary thrombocythemia
title Concomitant constitutive LNK and NFE2 mutation with loss of sumoylation in a case of hereditary thrombocythemia
title_full Concomitant constitutive LNK and NFE2 mutation with loss of sumoylation in a case of hereditary thrombocythemia
title_fullStr Concomitant constitutive LNK and NFE2 mutation with loss of sumoylation in a case of hereditary thrombocythemia
title_full_unstemmed Concomitant constitutive LNK and NFE2 mutation with loss of sumoylation in a case of hereditary thrombocythemia
title_short Concomitant constitutive LNK and NFE2 mutation with loss of sumoylation in a case of hereditary thrombocythemia
title_sort concomitant constitutive lnk and nfe2 mutation with loss of sumoylation in a case of hereditary thrombocythemia
topic Letters to the Editor
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8018143/
https://www.ncbi.nlm.nih.gov/pubmed/32554556
http://dx.doi.org/10.3324/haematol.2020.246587
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