Cargando…
Author Correction: Novel mutations in PIEZO1 cause an autosomal recessive generalized lymphatic dysplasia with non-immune hydrops fetalis
Autores principales: | Fotiou, Elisavet, Martin-Almedina, Silvia, Simpson, Michael A., Lin, Shin, Gordon, Kristiana, Brice, Glen, Atton, Giles, Jeffery, Iona, Rees, David C., Mignot, Cyril, Vogt, Julie, Homfray, Tessa, Snyder, Michael P., Rockson, Stanley G., Jeffery, Steve, Mortimer, Peter S., Mansour, Sahar, Ostergaard, Pia |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6486644/ https://www.ncbi.nlm.nih.gov/pubmed/31028252 http://dx.doi.org/10.1038/s41467-019-09905-4 |
Ejemplares similares
-
Novel mutations in PIEZO1 cause an autosomal recessive generalized lymphatic dysplasia with non-immune hydrops fetalis
por: Fotiou, Elisavet, et al.
Publicado: (2015) -
EPHB4 kinase–inactivating mutations cause autosomal dominant lymphatic-related hydrops fetalis
por: Martin-Almedina, Silvia, et al.
Publicado: (2016) -
Nonimmune hydrops fetalis due to autosomal recessive hereditary spherocytosis
por: Hannah, Dawn M., et al.
Publicado: (2017) -
hCALCRL mutation causes autosomal recessive nonimmune hydrops fetalis with lymphatic dysplasia
por: Mackie, Duncan I., et al.
Publicado: (2018) -
Thoracic Ganglioneuromas Resulting in Nonimmune Hydrops Fetalis
por: Singh, Paul, et al.
Publicado: (2014)