De novo novel splice‐site mutation in FLT4/VEGFR3 is associated with Milroy disease-Reference-Cited by-同舟云学术

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De novo novel splice‐site mutation in FLT4/VEGFR3 is associated with Milroy disease

Published:2020-09-29 Issue:1 Volume:48 Page:
ISSN:0385-2407
Container-title:The Journal of Dermatology
language:en
Short-container-title:J. Dermatol.

Author:

Shibata Yuka¹,Okamoto Toshio²,Saruta Takao³,Matsuoka Fumiya⁴,Fujieda Mikiya⁴,Sano Shigetoshi¹^ORCID

Affiliation:

1. Department of Dermatology Kochi Medical School Kochi University Nankoku Japan

2. Asahikawa Medical University Hospital Center for Maternity and Infant Care Asahikawa Japan

3. Saruta Skin Clinic Kochi Japan

4. Department of Pediatrics Kochi Medical School Kochi University Nankoku Japan

Publisher

Wiley

Subject

Dermatology,General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/1346-8138.15627

Reference5 articles.

1. Hereditary lymphedema: evidence for linkage and genetic heterogeneity

2. Expression of the fms-like tyrosine kinase 4 gene becomes restricted to lymphatic endothelium during development.

3. Milroy disease and the VEGFR-3 mutation phenotype

4. FLT4/VEGFR3and Milroy Disease: Novel Mutations, a Review of Published Variants and Database Update

5. Molecular characterization of two novel VEGFR3 mutations in Japanese families with Milroy’s disease

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. FLT4 Mutations Are Associated with Segmental Lymphatic Dysfunction and Initial Lymphatic Aplasia in Patients with Milroy Disease;Genes;2021-10-13

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