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LEPOARD syndrome: A report of a case with a novel PTPN11 mutation
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8054096/ https://www.ncbi.nlm.nih.gov/pubmed/33898683 http://dx.doi.org/10.1016/j.jdcr.2021.03.022 |
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author | Rahal, Nader Sadi, Amir Cohen-Barak, Eran Ziv, Michael Krausz, Judit Dodiuk-Gad, Roni P. |
author_facet | Rahal, Nader Sadi, Amir Cohen-Barak, Eran Ziv, Michael Krausz, Judit Dodiuk-Gad, Roni P. |
author_sort | Rahal, Nader |
collection | PubMed |
description | |
format | Online Article Text |
id | pubmed-8054096 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-80540962021-04-22 LEPOARD syndrome: A report of a case with a novel PTPN11 mutation Rahal, Nader Sadi, Amir Cohen-Barak, Eran Ziv, Michael Krausz, Judit Dodiuk-Gad, Roni P. JAAD Case Rep Case Report Elsevier 2021-03-20 /pmc/articles/PMC8054096/ /pubmed/33898683 http://dx.doi.org/10.1016/j.jdcr.2021.03.022 Text en © 2021 by the American Academy of Dermatology, Inc. Published by Elsevier, Inc. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Case Report Rahal, Nader Sadi, Amir Cohen-Barak, Eran Ziv, Michael Krausz, Judit Dodiuk-Gad, Roni P. LEPOARD syndrome: A report of a case with a novel PTPN11 mutation |
title | LEPOARD syndrome: A report of a case with a novel PTPN11 mutation |
title_full | LEPOARD syndrome: A report of a case with a novel PTPN11 mutation |
title_fullStr | LEPOARD syndrome: A report of a case with a novel PTPN11 mutation |
title_full_unstemmed | LEPOARD syndrome: A report of a case with a novel PTPN11 mutation |
title_short | LEPOARD syndrome: A report of a case with a novel PTPN11 mutation |
title_sort | lepoard syndrome: a report of a case with a novel ptpn11 mutation |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8054096/ https://www.ncbi.nlm.nih.gov/pubmed/33898683 http://dx.doi.org/10.1016/j.jdcr.2021.03.022 |
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