Homozygous p.D331Y mutation in PLA2G6 in two patients with pure autosomal-recessive early-onset parkinsonism: Further evidence of a fourth phenotype of PLA2G6-associated neurodegeneration

Fei Xie, Zhidong Cen, Zhiyuan Ouyang, Sheng Wu, Jianfeng Xiao, Wei Luo

Research output: Contribution to journalLetter

13 Citations (Scopus)
Original languageEnglish (US)
Pages (from-to)420-422
Number of pages3
JournalParkinsonism and Related Disorders
Volume21
Issue number4
DOIs
StatePublished - Apr 1 2015

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Group VI Phospholipases A2
Neuroaxonal Dystrophies
Consanguinity
Parkinsonian Disorders
Age of Onset
Phenotype
Mutation

All Science Journal Classification (ASJC) codes

  • Neurology
  • Geriatrics and Gerontology
  • Clinical Neurology

Cite this

Homozygous p.D331Y mutation in PLA2G6 in two patients with pure autosomal-recessive early-onset parkinsonism : Further evidence of a fourth phenotype of PLA2G6-associated neurodegeneration. / Xie, Fei; Cen, Zhidong; Ouyang, Zhiyuan; Wu, Sheng; Xiao, Jianfeng; Luo, Wei.

In: Parkinsonism and Related Disorders, Vol. 21, No. 4, 01.04.2015, p. 420-422.

Research output: Contribution to journalLetter

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AU - Cen, Zhidong

AU - Ouyang, Zhiyuan

AU - Wu, Sheng

AU - Xiao, Jianfeng

AU - Luo, Wei

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