File S1 - Revealing the Complexity of a Monogenic Disease: Rett Syndrome Exome Sequencing

Figshare2015-12-02 更新2026-04-29 收录

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Supporting methods, tables, references. Methods S1. Table S1, Variations predicted to impair protein function exclusive to classical RTT patients. Table S2, Variations predicted to impair protein function exclusive to Z-RTT patients. Table S3, Variations predicted to impair protein function in discordant RTT patients. References S1. (DOC)

创建时间：

2015-12-02