Exome sequencing in syndromic brain malformations identifies novel mutations in ACTB, and SLC9A6, and suggests BAZ1A as a new candidate gene
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| Description | scientific article published on 01 February 2018 |
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author: Bernhard Herrmann Heiko Reutter Ulrich Gembruch Amit Sharma |
| Publication date | February 1, 2018 |
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