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Identification of an HMGB3 Frameshift Mutation in a Family With an X-linked Colobomatous Microphthalmia Syndrome Using Whole-Genome and X-Exome Sequencing.
- Published in:
- JAMA Ophthalmology, 2014, v. 132, n. 10, p. 1215, doi. 10.1001/jamaophthalmol.2014.1731
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- Publication type:
- Article