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

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  • Affiliation of Author(s):基础医学院

  • Journal:Prenat Diagn.

  • All the Authors:gongyaoqin,Liu,shaochangshun

  • First Author:gongyaoqin

  • Document Code:lw-105535

  • Volume:30

  • Issue:5

  • Page Number:485

  • Number of Words:2500

  • Translation or Not:no

  • Date of Publication:2010-05-01

  • Date of Publication:2010-05-01
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