帕金森病
遗传学
复合杂合度
遗传分析
突变
营养不良
等位基因
生物
肌张力障碍
基因
遗传咨询
医学
疾病
病理
神经科学
作者
Saketh Kapoor,Mohd Hussain Shah,Nivedita Singh,Mohammad Iqbal Rather,Vishwanath Kumble Bhat,Sindhura Gopinath,Parayil Sankaran Bindu,Arun B. Taly,Sanjib Sinha,Madhu Nagappa,Rose Dawn Bharath,Anita Mahadevan,Narayanappa Gayathri,Yasha T. Chickabasaviah,Arun Kumar
出处
期刊:PLOS ONE
[Public Library of Science]
日期:2016-05-19
卷期号:11 (5): e0155605-e0155605
被引量:34
标识
DOI:10.1371/journal.pone.0155605
摘要
Mutations in PLA2G6 were identified in patients with a spectrum of neurodegenerative conditions, such as infantile neuroaxonal dystrophy (INAD), atypical late-onset neuroaxonal dystrophy (ANAD) and dystonia parkinsonism complex (DPC). However, there is no report on the genetic analysis of families with members affected with INAD, ANAD and DPC from India. Therefore, the main aim of this study was to perform genetic analysis of 22 Indian families with INAD, ANAD and DPC. DNA sequence analysis of the entire coding region of PLA2G6 identified 13 different mutations, including five novel ones (p.Leu224Pro, p.Asp283Asn, p.Arg329Cys, p.Leu491Phe, and p.Arg649His), in 12/22 (54.55%) families with INAD and ANAD. Interestingly, one patient with INAD was homozygous for two different mutations, p.Leu491Phe and p.Ala516Val, and thus harboured four mutant alleles. With these mutations, the total number of mutations in this gene reaches 129. The absence of mutations in 10/22 (45.45%) families suggests that the mutations could be in deep intronic or promoter regions of this gene or these families could have mutations in a yet to be identified gene. The present study increases the mutation landscape of PLA2G6. The present finding will be useful for genetic diagnosis, carrier detection and genetic counselling to families included in this study and other families with similar disease condition.
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