Affiliation of Author(s): : 基础医学院

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

Journal: : Prenat Diagn.

All the Authors: : gongyaoqin,Liu,shaochangshun

First Author: : gongyaoqin

Indexed by: : Unit Twenty Basic Research

Document Code: : lw-105535

Volume: : 30

Issue: : 5

Page Number: : 485

Translation or Not: : no

Date of Publication: : 2010-05-01