Bandah-Rozenfeld, D., Mizrahi-Meissonnier, L., Farhy, C., Obolensky, A., Chowers, I., Pe'er, J., . . . Sharon, D. (2010). Homozygosity Mapping Reveals Null Mutations in FAM161A as a Cause of Autosomal-Recessive Retinitis Pigmentosa. Elsevier.
Chicago Style CitationBandah-Rozenfeld, Dikla, et al. Homozygosity Mapping Reveals Null Mutations in FAM161A As a Cause of Autosomal-Recessive Retinitis Pigmentosa. Elsevier, 2010.
MLA CitationBandah-Rozenfeld, Dikla, et al. Homozygosity Mapping Reveals Null Mutations in FAM161A As a Cause of Autosomal-Recessive Retinitis Pigmentosa. Elsevier, 2010.
Warning: These citations may not always be 100% accurate.