A PHP Error was encountered

Severity: Warning

Message: fopen(/var/lib/php/sessions/ci_session815q7t18bmdvll9sb0ndcumhiup2k50r): Failed to open stream: No space left on device

Filename: drivers/Session_files_driver.php

Line Number: 177

Backtrace:

File: /var/www/html/index.php
Line: 316
Function: require_once

A PHP Error was encountered

Severity: Warning

Message: session_start(): Failed to read session data: user (path: /var/lib/php/sessions)

Filename: Session/Session.php

Line Number: 137

Backtrace:

File: /var/www/html/index.php
Line: 316
Function: require_once

A PHP Error was encountered

Severity: Warning

Message: file_get_contents(https://...@remsenmedia.com&api_key=81853a771c3a3a2c6b2553a65bc33b056f08&a=1): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests

Filename: helpers/my_audit_helper.php

Line Number: 197

Backtrace:

File: /var/www/html/application/helpers/my_audit_helper.php
Line: 197
Function: file_get_contents

File: /var/www/html/application/helpers/my_audit_helper.php
Line: 271
Function: simplexml_load_file_from_url

File: /var/www/html/application/helpers/my_audit_helper.php
Line: 3145
Function: getPubMedXML

File: /var/www/html/application/controllers/Detail.php
Line: 575
Function: pubMedSearch_Global

File: /var/www/html/application/controllers/Detail.php
Line: 489
Function: pubMedGetRelatedKeyword

File: /var/www/html/index.php
Line: 316
Function: require_once

SCA38 is rare in Mainland China. | LitMetric

SCA38 is rare in Mainland China.

J Neurol Sci

Department of Neurology, Xiangya Hospital, Central South University, Changsha, Hunan, PR China; Human Province Key Laboratory of Neurodegenerative Disorders, Changsha, Hunan, PR China; State Key Laboratory of Medical Genetics, Changsha, Hunan, PR China. Electronic address:

Published: November 2015

Spinocerebellar ataxias (SCAs) are a group of dominantly inherited neurodegenerative disorders distributed worldwide. Nearly 35 SCAs have been localized and 28 genes have been identified. Recently, mutations in the elongation of a very long chain fatty acids-5 gene (ELOVL5) were reported to cause a SCA38 subtype. To describe the epidemiology of SCA38 in Mainland China, we analyzed the coding sequence of ELOVL5 in 346 patients diagnosed as SCAs. Finally, we did not observe any disease-related gene mutations in ELOVL5. This suggests that the SCA38 subtype is very rare in Mainland China.

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.jns.2015.09.350DOI Listing

Publication Analysis

Top Keywords

mainland china
12
rare mainland
8
sca38 subtype
8
sca38
4
sca38 rare
4
china spinocerebellar
4
spinocerebellar ataxias
4
ataxias scas
4
scas group
4
group dominantly
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!