Identification and characterization of novel parathyroid-specific transcription factor Glial Cells Missing Homolog B (GCMB) mutations in eight families with autosomal recessive hypoparathyroidism
Bowl, Michael R., Mirczuk, Samantha M., Grigorieva, Irina V., Piret, Sian E., Cranston, Treena, Southam, Lorraine, Allgrove, Jeremy, Bahl, Shailini, Brain, Caroline, Loughlin, John, Mughal, Zulf, Ryan, Fiona, Shaw, Nick, Thakker, Yogini V., Tiosano, Dov, Nesbit, M. Andrew, Thakker, Rajesh V.
Published in Human molecular genetics (15.05.2010)
Published in Human molecular genetics (15.05.2010)
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