WP5381 - Smith-Magenis and Potocki-Lupski syndrome copy number variation - Homo sapiens
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https://www.ndexbio.org/viewer/networks/c7948a51-1438-11f0-9806-005056ae3c32
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资源简介：
The Smith-Magenis syndrome, is the result from a deletion of chr17:chr17:16,82-18,28, while the Potocki-Lupski syndrome is the result of a duplication of this area.
创建时间：
2025-04-17
