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In 2014, WES unveiled a variation in the GABRD gene in an RTT-like patient.https://t.co/0E8JqRMya5
In 2014, WES unveiled a variation in the GABRD gene in an RTT-like patient.https://t.co/0E8JqRMya5
RT @Exome_seq: The Utility of Next-Generation Sequencing in Gene Discovery for Mutation-Negative Patients with Rett Syndrome. http://t.co/X…
The Utility of Next-Generation Sequencing in Gene Discovery for Mutation-Negative Patients with Rett Syndrome. http://t.co/XXy09qiaUQ
The Utility of Next-Generation Sequencing in Gene Discovery for Mutation-Negative Patients with Rett Syndrome. http://t.co/FWgkdGJu1q