ARL2BP mutations account for 0.1% of autosomal recessive rod‐cone dystrophies with the report of a novel splice variant
I. Audo; S. El Shamieh; C. Méjécase; C. Michiels; V. Demontant; A. Antonio; C. Condroyer; F. Boyard; M. Letexier; J.‐P. Saraiva; S. Blanchard; S. Mohand‐Saïd; J.‐A. Sahel; C. Zeitz
Author Information: Department of Genetics
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