Download references

Open Access Highly Accessed

Mutations in LRP5 cause primary osteoporosis without features of OI by reducing Wnt signaling activity

Johanna Korvala, Harald Jüppner, Outi Mäkitie, Etienne Sochett, Dirk Schnabel, Stefano Mora, Cynthia F Bartels, Matthew L Warman, Donald Deraska, William G Cole, Heini Hartikka, Leena Ala-Kokko and Minna Männikkö*

BMC Medical Genetics 2012, 13:26 doi:10.1186/1471-2350-13-26

Include


Format