(Q50474860)
Statements
Functional analysis of a novel GATA3 mutation in a family with the hypoparathyroidism, deafness, and renal dysplasia syndrome (English)
Alireza Zahirieh
M Andrew Nesbit
Asif Ali
Kairong Wang
Ning He
Gerasimos Bamichas
Kostas Sombolos
York Pei
10 February 2005
2445-2450