Literature DB >> 29112699

Complicated hereditary spastic paraplegia due to ATP13A2 mutations: what's in a name?

Susanne de Bot1, Erik-Jan Kamsteeg2, Bart P C Van De Warrenburg3.   

Abstract

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Year:  2017        PMID： 29112699     DOI： 10.1093/brain/awx280

Source DB:  PubMed          Journal:  Brain        ISSN： 0006-8950            Impact factor:   13.501


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  4 in total

1.  Reply: Complicated hereditary spastic paraplegia due to ATP13A2 mutations: what's in a name?

Authors:  Rebecca Schüle
Journal:  Brain       Date:  2017-12-01       Impact factor: 13.501

2.  Autosomal Recessive Spastic Paraplegia Type 78 Associated with a Homozygous Variant in the ATP13A2 Gene.

Authors:  Hussein Algahtani; Bader Shirah; Salem Alshammari; Fareeda Alghamdi; Angham Abdulrhman Abdulkareem; Muhammad Imran Naseer
Journal:  Mov Disord Clin Pract       Date:  2022-07-12

3.  Identification of a novel mutation in ATP13A2 associated with a complicated form of hereditary spastic paraplegia.

Authors:  Yasuko Odake; Kishin Koh; Yoshihisa Takiyama; Hiroyuki Ishiura; Shoji Tsuji; Masahito Yamada; Mitsuhiro Yoshita
Journal:  Neurol Genet       Date:  2020-09-08

Review 4.  Challenges and Controversies in the Genetic Diagnosis of Hereditary Spastic Paraplegia.

Authors:  Lydia Saputra; Kishore Raj Kumar
Journal:  Curr Neurol Neurosci Rep       Date:  2021-02-28       Impact factor: 5.081
  4 in total

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