Parental mosaicism and autosomal dominant mutations causing structural abnormalities of collagen I are frequent in families with osteogenesis imperfecta type III/IV.
Autor: | Lund, AM, Nicholls, AC, Schwartz, M, Skovby, F, Lund, A M, Nicholls, A C |
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Zdroj: | Acta Paediatrica; Jul1997, Vol. 86 Issue 7, p711-718, 8p |
Databáze: | Complementary Index |
Externí odkaz: |