Cargando…
NOTCH1: Review of its role in lymphatic development and study of seven families with rare pathogenic variants
BACKGROUND: We developed a Next‐Generation‐Sequencing (NGS) protocol to screen the most frequent genetic variants related to lymphedema and a group of candidate genes. The aim of the study was to find the genetic cause of lymphedema in the analyzed patients. METHODS: We sequenced a cohort of 246 Ita...
Autores principales: | Michelini, Sandro, Ricci, Maurizio, Serrani, Roberta, Barati, Shila, Kenanoglu, Sercan, Veselenyiova, Dominika, Kurti, Danjela, Baglivo, Mirko, Basha, Syed Hussain, Priya, Sasi, Dautaj, Astrit, Dundar, Munis, Krajcovic, Juraj, Bertelli, Matteo |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7963424/ https://www.ncbi.nlm.nih.gov/pubmed/33247628 http://dx.doi.org/10.1002/mgg3.1529 |
Ejemplares similares
-
TIE1 as a Candidate Gene for Lymphatic Malformations with or without Lymphedema
por: Michelini, Sandro, et al.
Publicado: (2020) -
Two rare PROX1 variants in patients with lymphedema
por: Ricci, Maurizio, et al.
Publicado: (2020) -
Segregation Analysis of Rare NRP1 and NRP2 Variants in Families with Lymphedema
por: Michelini, Sandro, et al.
Publicado: (2020) -
Mutations in the ARAP3 Gene in Three Families with Primary Lymphedema Negative for Mutations in Known Lymphedema-Associated Genes
por: Ricci, Maurizio, et al.
Publicado: (2020) -
Neurobiological basis of chiropractic manipulative treatment of the spine in the care of major depression
por: Kiani, Aysha Karim, et al.
Publicado: (2020)