Cargando…
LEPOARD syndrome: A report of a case with a novel PTPN11 mutation
Autores principales: | Rahal, Nader, Sadi, Amir, Cohen-Barak, Eran, Ziv, Michael, Krausz, Judit, Dodiuk-Gad, Roni P. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
|
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 |
Ejemplares similares
-
Toxic epidermal necrolysis–like dermatomyositis associated with antimelanoma differentiation antigen 5
por: Kushnir-Grinbaum, Daniella, et al.
Publicado: (2018) -
Noonan syndrome: rhGH treatment and
PTPN11
mutation
por: Wu, Xian, et al.
Publicado: (2023) -
LEOPARD Syndrome with a Sporadic PTPN11 Mutation in a Saudi Patient
por: Alshamrani, Hussein M., et al.
Publicado: (2023) -
Cancer risk in patients with Noonan syndrome carrying a PTPN11 mutation
por: Jongmans, Marjolijn C J, et al.
Publicado: (2011) -
LEOPARD syndrome in an infant with severe hypertrophic cardiomyopathy and PTPN11 mutation
por: Ganigara, Madhusudan, et al.
Publicado: (2011)