山东大学教师主页 Yaoqin Gong Prenatal diagnosis of autosomal dominant hereditary spastic paraplegia (SPG42) caused by SLC33A1 mutation in a Chinese kindred. Home

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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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Institution: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.

First Author:Yaoqin Gong

All the Authors:刘奇迹,邵常顺,Yaoqin Gong

Document Code:lw-105535

Volume:30

Issue:5

Page Number:485

Number of Words:2500

Translation or Not:No

Date of Publication:2010-05

Release Time:2019-11-06

Pre One : A Missense Mutation in SLC33A1, which Encodes the Acetyl-CoA Transporter, Causes Autosomal-Dominant Spastic Paraplegia (SPG42).

Next One : A functional polymorphism in the SPINK5 gene is associated with asthma in a Chinese Han Population.

Personal information

Professor
Supervisor of Doctorate Candidates
Supervisor of Master's Candidates

Gender : Female

Alma Mater : 山东大学

Education Level : With Certificate of Graduation for Study as Master's Candidates

Degree : 博士

School/Department : 基础医学院

Date of Employment : 1985-10

Faculty/School : School of Basic Medical Sciences

Business Address : 趵突泉校区电镜楼211

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