Identification of a mutation causing deficient BMP1/mTLD proteolytic activity in autosomal recessive osteogenesis imperfecta

  1. Mart́inez-Glez, V.
  2. Valencia, M.
  3. Caparŕos-Mart́in, J.A.
  4. Aglan, M.
  5. Temtamy, S.
  6. Tenorio, J.
  7. Pulido, V.
  8. Lindert, U.
  9. Rohrbach, M.
  10. Eyre, D.
  11. Giunta, C.
  12. Lapunzina, P.
  13. Ruiz-Perez, V.L.
Aldizkaria:
Human Mutation

ISSN: 1098-1004 1059-7794

Argitalpen urtea: 2012

Alea: 33

Zenbakia: 2

Orrialdeak: 343-350

Mota: Artikulua

DOI: 10.1002/HUMU.21647 GOOGLE SCHOLAR