reference/12010593

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publicationName	The American Journal of Human Genetics
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bibliographicCitation	Weedon M, Hastings R, Caswell R, Xie W, Paszkiewicz K, Antoniadi T, Williams M, King C, Greenhalgh L, Newbury-Ecob R, Ellard S. Exome Sequencing Identifies a DYNC1H1 Mutation in a Large Pedigree with Dominant Axonal Charcot-Marie-Tooth Disease. The American Journal of Human Genetics. 2011 Aug;89(2):308–12. doi: 10.1016/j.ajhg.2011.07.002.
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date	2011-08-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://doi.org/10.1016/j.ajhg.2011.07.002 https://pubmed.ncbi.nlm.nih.gov/21820100 https://pubmed.ncbi.nlm.nih.gov/PMC3155164
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language	English
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title	Exome Sequencing Identifies a DYNC1H1 Mutation in a Large Pedigree with Dominant Axonal Charcot-Marie-Tooth Disease
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