(Q51139805)
Statements
1 reference
A novel deletion mutation involving TMEM38B in a patient with autosomal recessive osteogenesis imperfecta. (English)
1 reference
1 reference
1 reference
Elisa Rubinato
1 reference
Anna Morgan
1 reference
Angela D'Eustacchio
1 reference
Giulia Gortani
1 reference
Paolo Gasparini
1 reference
14 May 2014
1 reference
1 reference
545
1 reference
2
1 reference
290-292
1 reference
Identifiers
1 reference