Arg(1809) substitution in neurofibromin: further evidence of a genotype–phenotype correlation in neurofibromatosis type 1

Παρόμοια τεκμήρια

• Whole exome sequencing identifies MRVI1 as a susceptibility gene for moyamoya syndrome in neurofibromatosis type 1.
  ανά: Claudia Santoro, κ.ά.
  Έκδοση: (2018-01-01)
• Whole exome sequencing identifies MRVI1 as a susceptibility gene for moyamoya syndrome in neurofibromatosis type 1
  ανά: Santoro, Claudia, κ.ά.
  Έκδοση: (2018)
• Seizures in children with neurofibromatosis type 1: is neurofibromatosis type 1 enough?
  ανά: Santoro, Claudia, κ.ά.
  Έκδοση: (2018)
• p.Arg1809Cys substitution in neurofibromin is associated with a distinctive NF1 phenotype without neurofibromas
  ανά: Pinna, Valentina, κ.ά.
  Έκδοση: (2015)
• Clinical and Genetic Findings in Children with Neurofibromatosis Type 1, Legius Syndrome, and Other Related Neurocutaneous Disorders
  ανά: Giugliano, Teresa, κ.ά.
  Έκδοση: (2019)