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...
Prif Awduron: | Edwards, T, Williams, J, Patrício, M, Simunovic, M, Shanks, M, Clouston, P, MacLaren, R |
---|---|
Fformat: | Journal article |
Iaith: | English |
Cyhoeddwyd: |
Wiley
2017
|
Eitemau Tebyg
-
The spectrum of CHM gene mutations in choroideremia and their relationship to clinical phenotype
gan: Simunovic, M, et al.
Cyhoeddwyd: (2016) -
Choroideremia: molecular mechanisms and development of AAV gene therapy
gan: Patrício, M, et al.
Cyhoeddwyd: (2018) -
Prenylation of rab6a as a potency assay for choroideremia gene therapy
gan: Patricio, M, et al.
Cyhoeddwyd: (2017) -
Recent advances and future prospects in choroideremia
gan: Zinkernagel MS, et al.
Cyhoeddwyd: (2015-11-01) -
Macular hole surgery in patients with end-stage choroideremia
gan: Zinkernagel, MS, et al.
Cyhoeddwyd: (2013)