Homozygous deletion mutation of the parkin gene in patients with atypical parkinsonism

Antzeko izenburuak

• Three parkin gene mutations in a sibship with autosomal recessive early onset parkinsonism
  nork: Bonifati, V, et al.
  Argitaratua: (2001)
• A Case of Parkinson's Disease with No Lewy Body Pathology due to a Homozygous Exon Deletion in Parkin
  nork: Johansen, Krisztina Kunszt, et al.
  Argitaratua: (2018)
• Mutational screening of the parkin gene among South Indians with early onset Parkinson's disease
  nork: Madegowda, R, et al.
  Argitaratua: (2005)
• Relative high frequency of the c.255delA parkin gene mutation in Spanish patients with autosomal recessive parkinsonism
  nork: Munoz, E, et al.
  Argitaratua: (2002)
• Homozygous Deletion Mutation of the FERMT1 Gene in a Chinese Patient with Kindler Syndrome
  nork: Oh, Seung Joon, et al.
  Argitaratua: (2016)