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...

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Detalles Bibliográficos
Autores principales: Sui, Yu, Lu, Yongping, Lin, Meina, Ni, Xiang, Chen, Xinren, Li, Huan, Jiang, Miao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Research
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

Internet

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

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