Genetic Disorders of Parathyroid Development and Function
Author:
Funder
NIH
Publisher
Elsevier BV
Subject
Endocrinology,Endocrinology, Diabetes and Metabolism
Reference85 articles.
1. Familial isolated hypoparathyroidism caused by a mutation in the gene for the transcription factor GCMB;Ding;J Clin Invest,2001
2. Gcm2 is required for the differentiation and survival of parathyroid precursor cells in the parathyroid/thymus primordia;Liu;Dev Biol,2007
3. Identification and characterization of novel parathyroid-specific transcription factor Glial Cells Missing Homolog B (GCMB) mutations in eight families with autosomal recessive hypoparathyroidism;Bowl;Hum Mol Genet,2010
4. Glial cells missing-2 (GCM2) transactivates the calcium-sensing receptor gene: effect of a dominant-negative GCM2 mutant associated with autosomal dominant hypoparathyroidism;Canaff;Hum Mutat,2009
5. A missense glial cells missing homolog B (GCMB) mutation, Asn502His, causes autosomal dominant hypoparathyroidism;Mirczuk;J Clin Endocrinol Metab,2010
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