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Whole-Exome Sequencing Identifies LRIT3 Mutations as a Cause of Autosomal-Recessive Complete Congenital Stationary Night Blindness
Authors: Zeitz, Christina Jacobson, Samuel G. Hamel, Christian P. Bujakowska, Kinga
Citation: Zeitz, Christina et al., Whole-Exome Sequencing Identifies LRIT3 Mutations as a Cause of Autosomal-Recessive Complete Congenital Stationary Night Blindness, American journal of human genetics (Online) AJHG , 92(1), 2013, pp. 67-75
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