Clinical features associated with CTNNB1 de novo loss of function mutations in ten individuals
Autor: | Kharbanda, Mira, Pilz, Daniela T., Tomkins, Susan, Chandler, Kate, Saggar, Anand, Fryer, Alan, McKay, Victoria, Louro, Pedro, Smith, Jill Clayton, Burn, John, Kini, Usha, De Burca, Anna, FitzPatrick, David R., Kinning, Esther |
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Zdroj: | In European Journal of Medical Genetics February 2017 60(2):130-135 |
Databáze: | ScienceDirect |
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