eP095: A family-based study of hereditary spastic paraplegia type 46 in two siblings due to a novel GBA2 variant

Abstract

Open access

Peer reviewed

Bharatendu Chandra, Shelby Romoser, Jaclyn Kotlarek, Taylor Warner and Hatem El-Shanti

Genetics in medicine, Vol.24(3), pp.S62-S62

03/2022

DOI: 10.1016/j.gim.2022.01.132

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https://doi.org/10.1016/j.gim.2022.01.132View

Published (Version of record) Open Access

Title: Subtitle: eP095: A family-based study of hereditary spastic paraplegia type 46 in two siblings due to a novel GBA2 variant
Creators: Bharatendu Chandra - University of Iowa
Shelby Romoser - University of Iowa
Jaclyn Kotlarek - University of Iowa
Taylor Warner - University of Iowa
Hatem El-Shanti - University of Iowa
Resource Type: Abstract
Publication Details: Genetics in medicine, Vol.24(3), pp.S62-S62
Publisher: Elsevier Inc
DOI: 10.1016/j.gim.2022.01.132
ISSN: 1098-3600
eISSN: 1530-0366
Language: English
Date published: 03/2022
Academic Unit: Stead Family Department of Pediatrics; Medical Genetics and Genomics
Record Identifier: 9984354398702771

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