Phenotypic characterization of a large family with RP10 autosomal-dominant retinitis pigmentosa: an Asp226Asn mutation in the IMPDH1 gene.
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G. Fish | S. Daiger | S. Bowne | L. Sullivan | D. Birch | K. Locke | P. Kozma | D. Hughbanks-Wheaton | Anisa I. Gire | C. J. Spellicy | S. J. Bowne | Catherine J. Spellicy