Genetic variants that cause brachydactyly type B
收藏NIAID Data Ecosystem2026-03-13 收录
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https://www.ncbi.nlm.nih.gov/bioproject/PRJNA868321
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资源简介：
Brachydactyly type B1 (BDB1) is the most severe form of brachydactyly and is caused by truncating variations in the receptor tyrosine kinase like orphan receptor 2, or ROR2 gene. The aim of our study was to identify the gene variants in families with BDB1.
创建时间：
2022-08-10
