Mild dominant osteogenesis imperfecta with intrafamilial variability: the cause is a serine for glycine ?1(I) 901 substitution in a type-I collagen gene
1992; Springer Science+Business Media; Volume: 89; Issue: 5 Linguagem: Inglês
10.1007/bf00219169
ISSN1432-1203
AutoresMonica Mottes, Antonella Sangalli, Maurizia Valli, Macarena Gomez‐Lira, Ruggero Tenni, P Buttitta, PierFranco Pignatti, Giuseppe Cetta,
Tópico(s)Wnt/β-catenin signaling in development and cancer
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