Exome sequencing of two patients in a family with atypical X-linked leukodystrophy
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.2011.01721.x/fullpdf
Reference13 articles.
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4. Novel genomic techniques open new avenues in the analysis of monogenic disorders.;Kuhlenbaumer;Hum Mutat,2011
5. Loss-of-function mutations of CHST14 in a new type of Ehlers-Danlos syndrome.;Miyake;Hum Mutat,2010
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