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Germline Mutations Affecting Gα<sub>11</sub> in Hypoparathyroidism
Journal article published in 2013 by
Michael Mannstadt,
Mark Harris,
Bert Bravenboer,
Sridhar Chitturi,
Koen M. A. Dreijerink,
David G. Lambright,
Elaine T. Lim 
,
Mark J. Daly,
Stacey Gabriel,
Harald Jüppner
,
Mark J. Daly,
Stacey Gabriel,
Harald Jüppner
Abstract
In a study reported here, genomewide linkage analysis and whole-exome sequencing were used to identify two different heterozygous Gα11 mutations in autosomal-dominant, isolated hypoparathyroidism.