Prenatal diagnosis of autosomal dominant hereditary spastic paraplegia (SPG42) caused by SLC33A1 mutation in a Chinese kindred

  • Pengfei Lin
  • , Fei Mao
  • , Qiji Liu
  • , Changshun Shao
  • , Chuanzhu Yan
  • , Yaoqin Gong

Research output: Contribution to journalArticlepeer-review

10 Scopus citations
Original languageEnglish
Pages (from-to)485-486
Number of pages2
JournalPrenatal Diagnosis
Volume30
Issue number5
DOIs
StatePublished - May 2010
Externally publishedYes

Keywords

  • Gene diagnosis
  • Hereditary spastic paraplegia
  • Mutation detection
  • SLC33A1

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