☆ 4.4 Letter

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

PRENATAL DIAGNOSIS (2010)

Journal

PRENATAL DIAGNOSIS

Volume 30, Issue 5, Pages 485-486

Publisher

WILEY

DOI: 10.1002/pd.2485

Keywords

hereditary spastic paraplegia; SLC33A1; gene diagnosis; mutation detection

Categories

Genetics & Heredity Obstetrics & Gynecology

Ask authors/readers for more resources

Protocol

Community support

Reagent

Community support

Authors

I am an author on this paper

Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.4

Not enough ratings

Secondary Ratings

Novelty

-

Significance

-

Scientific rigor

-

Rate this paper

Recommended

No Data Available

No Data Available

No Data Available

© Peeref 2019-2024. All rights reserved.