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Mutations in the gene LEMD3 in patients with osteopoikilosis and melorheostosis - Evidence for genetic heterogeneity

Mutations in the gene LEMD3 in patients with osteopoikilosis and melorheostosis - Evidence for genetic heterogeneity

Detalhes bibliográficos
Main Authors: Couto, A, Armas, J, Brown, M, Peach, C, Wordsworth, P, Zhang, Y
Formato: Conference item
Publicado em: 2006
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Registos relacionados

  • A novel LEMD3 mutation common to patients with osteopoikilosis with and without melorheostosis.
    Por: Couto, A, et al.
    Publicado em: (2007)
  • Novel and recurrent germline LEMD3 mutations causing Buschke-Ollendorff syndrome and osteopoikilosis but not isolated melorheostosis.
    Por: Zhang, Y, et al.
    Publicado em: (2009)
  • A novel LEMD3 pathogenic variant in a son and mother with osteopoikilosis
    Por: Selin Elmaoğulları, et al.
    Publicado em: (2019-08-01)
  • Osteopoikilosis and multiple exostoses caused by novel mutations in <it>LEMD3 </it>and <it>EXT1 </it>genes respectively - coincidence within one family
    Por: Horn Denise, et al.
    Publicado em: (2010-07-01)
  • Mutation in LEMD3 (Man1) Associated with Osteopoikilosis and Late-Onset Generalized Morphea: A New Buschke-Ollendorf Syndrome Variant
    Por: Benjamin Korman, et al.
    Publicado em: (2016-01-01)

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