A large homozygous or heterozygous in-frame deletion within the calcium-sensing receptor's carboxylterminal cytoplasmic tail that causes autosomal dominant hypocalcemia (Q40886257)
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| Language | Label | Description | Also known as |
|---|---|---|---|
| English | A large homozygous or heterozygous in-frame deletion within the calcium-sensing receptor's carboxylterminal cytoplasmic tail that causes autosomal dominant hypocalcemia |
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A large homozygous or heterozygous in-frame deletion within the calcium-sensing receptor's carboxylterminal cytoplasmic tail that causes autosomal dominant hypocalcemia (English)
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Lienhardt A
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Garabédian M
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Bai M
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Sinding C
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Zhang Z
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Lagarde JP
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Boulesteix J
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Rigaud M
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Brown EM
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Kottler ML
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1 April 2000
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