WP5408 - 15q25 copy number variation - Homo sapiens
收藏NIAID Data Ecosystem2026-05-02 收录
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15q25.2 or generally 15q25 copy number variations are rare genetic disorders that cause neuropsychiatric disorders, developmental delay and cardiac abnormalities. The exact chromosomal position for this pathway (chr15:83219735-85722039, GRCh37) was taken from Kirov et al. 2014 10.1016/j.biopsych.2013.07.022 and literature cited there.
创建时间：
2025-04-17
