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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. [electronic resource] by
- Lienhardt, A
- Garabédian, M
- Bai, M
- Sinding, C
- Zhang, Z
- Lagarde, J P
- Boulesteix, J
- Rigaud, M
- Brown, E M
- Kottler, M L
Producer: 20000501
In:
The Journal of clinical endocrinology and metabolism vol. 85
Availability: No items available.
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