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A family with Milroy disease caused by the FLT4/VEGFR3 gene variant c.2774 T > A
BACKGROUND: Milroy disease (MD) is a rare, autosomal-dominant disorder. Variants in the Fms-related tyrosine kinase 4 (FLT4/VEGFR3) gene cause the symptoms of this disease. In this report, we investigated the variant in a large Chinese family with MD. METHODS: We conducted Sanger sequencing of exons...
| Autores principales: | , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
BioMed Central
2021
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8186030/ https://www.ncbi.nlm.nih.gov/pubmed/34103024 http://dx.doi.org/10.1186/s12920-021-00997-w |