Erratum: Mutation Analysis of SPAST, ATL1, and REEP1 in Korean Patients with Hereditary Spastic Paraplegia

(1)

376 The publisher wishes to apologize for incorrectly displaying Fig. 1 and its legend.

So corrected figure and its legend should be as follows;

Erratum: Mutation Analysis of SPAST, ATL1, and REEP1 in Korean Patients with Hereditary Spastic Paraplegia

Tae-Hyoung Kim,

^a,b

Jae-Hyeok Lee,

^a,b

Young-Eun Park,

^a

Jin-Hong Shin,

^a,b

Tai-Seung Nam,

^c

Hyang-Sook Kim,

^b

Ho-Jung Jang,

^b

Artem Semenov,

^b

Sang Jin Kim,

^d

Dae-Seong Kim

^a,b

aDepartment of Neurology, Pusan National University School of Medicine, Yangsan, Korea

bResearch Institute for Convergence of Biomedical Science and Technology, Pusan National University Yangsan Hospital, Yangsan, Korea

cDepartment of Neurology, Chonnam National University Hospital, Gwangju, Korea

dDepartment of Neurology, Busan Paik Hospital, Inje University College of Medicine, Busan, Korea J Clin Neurol 2014;10(3):257-261

http://dx.doi.org/10.3988/jcn.2014.10.3.257

Print ISSN 1738-6586 / On-line ISSN 2005-5013 http://dx.doi.org/10.3988/jcn.2014.10.4.376 ERRATUM

J Clin Neurol 2014;10(4):376-376

Open Access

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Fig. 1. Organization of spastin and loca- tion of SPAST mutations identified in Korean HSP patients. *Nonsense mutations. Novel mutations are shown in bold- face. AAA: ATPases Associated with a wide variety of Activities, HD: hydropho- bic domain, HSP: hereditary spastic paraplegia, MIT: microtubule interacting and trafficking domain, MTBD: microtubule bi- nding domain.

p.S44*

p.S245*

c.870+3A>G p.L426fs*16

c.1413+3delAAGT p.D584V p.T550fs*14 p.R499H p.L379_L380del

p.F404del p.T369P p.I344K p.I127Tfs*35

HD MIT

MTBD

AAA p.K254*

p.S399L p.R451del

p.S458R

p.R499H p.R581* In our study

In previous Korean studies p.R372G