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Functional analysis of a novel GATA3 mutation in a family with the hypoparathyroidism, deafness, and renal dysplasia syndrome. [electronic resource] by
- Zahirieh, Alireza
- Nesbit, M Andrew
- Ali, Asif
- Wang, Kairong
- He, Ning
- Stangou, Maria
- Bamichas, Gerasimos
- Sombolos, Kostas
- Thakker, Rajesh V
- Pei, York
Producer: 20050531
In:
The Journal of clinical endocrinology and metabolism vol. 90
Availability: No items available.
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