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Kobayashi, H., Kasahara, M., Hino, M. et al. A novel heterozygous deletion frameshift mutation of GATA3 in a Japanese kindred with the hypoparathyroidism, deafness and renal dysplasia syndrome. J Endocrinol Invest 29, 851–853 (2006). https://doi.org/10.1007/BF03347383
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DOI: https://doi.org/10.1007/BF03347383