Impaired growth and intracranial calcifications in autosomal dominant hypocalcemia caused by a GNA11 mutation.
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Autosomal Dominant Hypocalcemia (Hypoparathyroidism) Types 1 and 2Knockin mouse with mutant Gα11 mimics human inherited hypocalcemia and is rescued by pharmacologic inhibitors.Gα11 mutation in mice causes hypocalcemia rectifiable by calcilytic therapy.Diseases associated with calcium-sensing receptorHypoparathyroidism.
P2860
Impaired growth and intracranial calcifications in autosomal dominant hypocalcemia caused by a GNA11 mutation.
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article científic
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article scientifique
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articolo scientifico
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artigo científico
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bilimsel makale
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scientific article published on 22 June 2016
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
Impaired growth and intracrani ...... ia caused by a GNA11 mutation.
@en
Impaired growth and intracrani ...... ia caused by a GNA11 mutation.
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type
label
Impaired growth and intracrani ...... ia caused by a GNA11 mutation.
@en
Impaired growth and intracrani ...... ia caused by a GNA11 mutation.
@nl
prefLabel
Impaired growth and intracrani ...... ia caused by a GNA11 mutation.
@en
Impaired growth and intracrani ...... ia caused by a GNA11 mutation.
@nl
P2093
P2860
P356
P1476
Impaired growth and intracrani ...... ia caused by a GNA11 mutation.
@en
P2093
Harald Jüppner
Monica Reyes
Outi Mäkitie
Sanna Toiviainen-Salo
Sirpa Tenhola
P2860
P304
P356
10.1530/EJE-16-0109
P577
2016-06-22T00:00:00Z