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Coexistence of two different pseudohypoparathyroidism subtypes (Ia and Ib) in the same kindred with independent Gsα coding mutations and GNAS imprinting defects
- Correspondence to Guiomar Perez de Nanclares, Molecular Genetics Laboratory Research Unit, Hospital Txagorritxu, Vitoria-Gasteiz, E01009 Alava, Basque Country, Spain; gnanclares{at}osakidetza.net
- Murat Bastepe, Endocrine Unit, Massachusetts General Hospital, 50 Blossom Street, Thier 10, Boston, Massachussetts 02114, USA; bastepe{at}helix.mgh.harvard.edu
Citation
Coexistence of two different pseudohypoparathyroidism subtypes (Ia and Ib) in the same kindred with independent Gsα coding mutations and GNAS imprinting defects
Publication history
- Received July 7, 2009
- Revised September 25, 2009
- Accepted September 28, 2009
- First published October 26, 2009.
Online issue publication
April 27, 2016
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© 2009, Published by the BMJ Publishing Group Limited For permission to use, (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions.