WP4950 - 16p11.2 distal deletion syndrome - Homo sapiens
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https://www.ndexbio.org/viewer/networks/a20e190f-5c73-11ec-b3be-0ac135e8bacf
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资源简介：
16p11.2 distal deletion syndrome is a rare genetic disorder (copy number variation) caused by a deletion on chromosome 16 in the range 28.74-28.95-Mb. The breakpoints in this pathway are chr16:28,823,196-29,046,783 (GHCh37) from Kendall et al. 2017 https://doi.org/10.1016/j.biopsych.2016.08.014.
创建时间：
2025-04-17
