A family with Milroy disease caused by the FLT4/VEGFR3 gene variant c.2774 T > A
Abstract 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 o...
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| Main Authors: | , , , , , , |
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| Format: | Book |
| Published: |
BMC,
2021-06-01T00:00:00Z.
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| Online Access: | Connect to this object online. |
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