First case of Roma ethnic origin with Andermann syndrome: A novel frameshift mutation in exon 20 of SLC12A6 gene

Author:

Pacheva Iliyana12ORCID,Todorov Tihomir3,Halil Zeyra1,Yordanova Ralitsa12,Todorova Albena34,Geneva Ina12,Galabova Fani2,Ivanov Ivan12

Affiliation:

1. Department of Pediatrics and Medical GeneticsMedical University Plovdiv Bulgaria

2. Department of PediatricsUniversity Hospital, St. George Plovdiv Bulgaria

3. Genetic Medico‐Diagnostic Laboratory “Genica” Sofia Bulgaria

4. Department of Medical Chemistry and BiochemistryMedical University Sofia Bulgaria

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference27 articles.

1. A new splice-site mutation in SLC12A6 causing Andermann syndrome with motor neuronopathy

2. Handbook of clinical neurology 1981 North‐Holland Amsterdam E. Andermann M. Teopoulos Sensorimotor neuronopathy with agenesis of the corpus callosum 100 103

3. Three familial midline malformtion syndromes of the central nervous system: Agenesis of the corpus callosum and anterior horn‐cell disease; agenesis of cerebellar vermis; and atrophy of the cerebellar vermis;Andermann E.;Birth Defects Original Article Series,1975

4. Familial agenesis of the corpus callosum with anterior horn cell disease. A syndrome of mental retardation, areflexia and paraparesis;Andermann F.;Transactions of the American Neurological Association,1972

Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3