Identification and characterization of novel parathyroid-specific transcription factor Glial Cells Missing Homolog B (GCMB) mutations in eight families with autosomal recessive hypoparathyroidism
Work
Year: 2010
Type: article
Source: Human Molecular Genetics
Authors Michael R. Bowl, Samantha Mirczuk, I. V. Grigorieva, Siân E. Piret, Treena Cranston +12 more
Institutions Churchill Hospital, University of Oxford, Oxford Centre for Diabetes, Endocrinology and Metabolism, Nuffield Orthopaedic Centre, Great Ormond Street Hospital +8 more
Cites: 41
Cited by: 48
Related to: 10
FWCI: 2.14
Citation percentile (by year/subfield): 90.48
Subfield: Genetics
Domain: Life Sciences
Open Access status: closed