An autosomal homologue of the choroideremia gene colocalizes with the usher syndrome type II locus on the distal part of chromosome 1q

Author:

Cremers Frans P.M.,Molloy Catherine M.,van de Pol Dorien J.R.,Hurk José A.J.M.van den,Bach Irene,Kessel Ad H.M.Geurts van,Ropers Hans-Hilger

Publisher

Oxford University Press (OUP)

Subject

Genetics(clinical),Genetics,Molecular Biology,General Medicine

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4. Molecular Therapy for Choroideremia: Pre-clinical and Clinical Progress to Date;Molecular Diagnosis & Therapy;2021-10-18

5. CHMmutation spectrum and disease: An update at the time of human therapeutic trials;Human Mutation;2021-02-19

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