A Novel Frameshift Mutation in Neurofibromin 1 Gene in a Chinese Family with Neurofibromatosis Type 1

Lignende værker

• Rs3213758 in the RPGRIP1L Gene Associated with Susceptibility to Segmental Vitiligo in a Chinese Han Population
  af: Hu, Man, et al.
  Udgivet: (2018)
• Elucidating the impact of neurofibromatosis-1 germline mutations on neurofibromin function and dopamine-based learning
  af: Anastasaki, Corina, et al.
  Udgivet: (2015)
• Four frameshift mutations in neurofibromatosis type 1 caused by small insertions.
  af: Colman, S D, et al.
  Udgivet: (1997)
• A clinical variant of neurofibromatosis type 1: familial spinal neurofibromatosis with a frameshift mutation in the NF1 gene.
  af: Ars, E, et al.
  Udgivet: (1998)
• Identification of a Novel NF1 Frameshift Variant in a Chinese Family with Neurofibromatosis Type 1
  af: Xu, Guoyao, et al.
  Udgivet: (2019)