Juvenile Paget’s Disease With Heterozygous Duplication In TNFRSF11A Encoding RANK

Ítems similars

• Juvenile Paget’s Disease In An Iranian Kindred With Vitamin D Deficiency And Novel Homozygous TNFRSF11B Mutation
  per: Saki, Forough, et al.
  Publicat: (2013)
• Early-Onset Paget’s Disease of Bone in a Mexican Family Caused by a Novel Tandem Duplication (77dup27) in TNFRSF11A that Encodes RANK
  per: Iwamoto, Sean J., et al.
  Publicat: (2020)
• Juvenile Paget’s Disease From Heterozygous Mutation of SP7 Encoding Osterix (Specificity Protein 7, Transcription Factor Sp7)
  per: Whyte, Michael P., et al.
  Publicat: (2020)
• Auricular Ossification: A Newly Recognized Feature of Osteoprotegerin-Deficiency Juvenile Paget Disease
  per: Gottesman, Gary S., et al.
  Publicat: (2016)
• Camurati-Engelmann Disease: Unique Variant Featuring a Novel Mutation in TGFβ1 Encoding Transforming Growth Factor Beta 1 and a Missense Change in TNFSF11 Encoding RANK Ligand
  per: Whyte, Michael P, et al.
  Publicat: (2011)