Gain-of-Function Mutations in G alpha 11 Cause a Novel Form of Autosomal-Dominant Hypoparathyroidism

Mannstadt, M; Nesbit, M; Howles, S; Rogers, A; Thakker, R; Jueppner, H

Journal article

Gain-of-Function Mutations in G alpha 11 Cause a Novel Form of Autosomal-Dominant Hypoparathyroidism

Publication status:: Published

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APA Style

Mannstadt, M., Nesbit, M., Howles, S., Rogers, A., Thakker, R., & Jueppner, H. (2013). Gain-of-Function Mutations in G alpha 11 Cause a Novel Form of Autosomal-Dominant Hypoparathyroidism. JOURNAL OF BONE AND MINERAL RESEARCH, 28.

MLA Style

Mannstadt, M., et al. “Gain-of-Function Mutations in G Alpha 11 Cause a Novel Form of Autosomal-Dominant Hypoparathyroidism.” JOURNAL OF BONE AND MINERAL RESEARCH, vol. 28, 2013.

Chicago Style

Mannstadt, M, M Nesbit, S Howles, A Rogers, R Thakker, and H Jueppner. 2013. “Gain-of-Function Mutations in G Alpha 11 Cause a Novel Form of Autosomal-Dominant Hypoparathyroidism.” JOURNAL OF BONE AND MINERAL RESEARCH 28.
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+ Mannstadt, M More by this author

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+ Nesbit, M More by this author

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University of Oxford

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MSD

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RDM

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OCDEM

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+ Howles, S More by this author

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+ Rogers, A More by this author

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+ Thakker, R More by this author

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Bibliographic Details

Journal:: JOURNAL OF BONE AND MINERAL RESEARCH
Volume:: 28
Publication date:: 2013-02-01
ISSN:: 0884-0431

Item Description

Pubs id:: pubs:470519
UUID:: uuid:b7cf4fc7-5995-430a-820f-517d7755b473
Local pid:: pubs:470519
Source identifiers:: 470519
Deposit date:: 2014-08-21

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Journal article

Gain-of-Function Mutations in G alpha 11 Cause a Novel Form of Autosomal-Dominant Hypoparathyroidism

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