Novel non-contiguous exon duplication in choroideremia

The importance of establishing a genetic diagnosis in patients with a choroideremia phenotype has been underscored by the advent of gene replacement therapy for this condition. Here, we describe a complex imbalance at the CHM locus in a male patient with classical disease. At the DNA level, this imb...

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מידע ביבליוגרפי
Main Authors: Edwards, T, Williams, J, Patrício, M, Simunovic, M, Shanks, M, Clouston, P, MacLaren, R
פורמט: Journal article
שפה:English
יצא לאור: Wiley 2017