Mutations in FKBP10 cause both Bruck syndrome and isolated osteogenesis imperfecta in humans (Q55982308)
Jump to navigation
Jump to search
No description defined
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Mutations in FKBP10 cause both Bruck syndrome and isolated osteogenesis imperfecta in humans |
No description defined |
Statements
Mutations in FKBP10 cause both Bruck syndrome and isolated osteogenesis imperfecta in humans (English)
0 references
12 May 2011
0 references
155
0 references
6
0 references
1448-1452
0 references
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference