File S1 - Revealing the Complexity of a Monogenic Disease: Rett Syndrome Exome Sequencing
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https://figshare.com/articles/dataset/Revealing_the_Complexity_of_a_Monogenic_Disease_Rett_Syndrome_Exome_Sequencing__/641765
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资源简介：
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.
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创建时间：
2013-03-01
