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Identification and characterization of novel parathyroid-specific transcription factor Glial Cells Missing Homolog B (GCMB) mutations in eight families with autosomal recessive hypoparathyroidism
Bowl, M. R., Mirczuk, S. M., Grigorieva, I. V., Piret, S. E., Cranston, T., Southam, L., Allgrove, J., Bahl, S., Brain, C., Loughlin, J., Mughal, Z., Ryan, F., Shaw, N., Thakker, Y. V., Tiosano, D., NVolume:
19
Language:
english
Journal:
Human Molecular Genetics
DOI:
10.1093/hmg/ddq084
Date:
May, 2010
File:
PDF, 462 KB
english, 2010