A novel mutation in the GCM2 gene causing severe congenital isolated hypoparathyroidism.
Doyle, Daniel; Kirwin, Susan M.; Sol-Church, Katia; Levine, Michael A.; Journal of Pediatric Endocrinology & Metabolism, 2012, vol. 25, issue 7/8, p 741, ISSN 0334018x. ISBN 0334018x.

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