Long-term clinical outcome and carrier phenotype in autosomal recessive hypophosphatemia caused by a novel DMP1 mutation


Mäkitie O., Pereira R. C., Kaitila I., Turan S., Bastepe M., Laine T., ...Daha Fazla

Journal of Bone and Mineral Research, cilt.25, sa.10, ss.2165-2174, 2010 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 25 Sayı: 10
  • Basım Tarihi: 2010
  • Doi Numarası: 10.1002/jbmr.105
  • Dergi Adı: Journal of Bone and Mineral Research
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.2165-2174
  • Anahtar Kelimeler: HYPOPHOSPHATEMIA, RICKETS, OSTEOMALACIA, SKELETAL DYSPLASIA, DMP1, FGF-23, MATRIX PROTEIN-1 DMP1, IN-VIVO, MARFAN-SYNDROME, BONE, OSTEOMALACIA, RICKETS, FGF23, MICE
  • Marmara Üniversitesi Adresli: Evet