Twelve Novel Single Nucleotide Polymorphisms in ABCB1/MDR1 among Japanese Patients with Ventricular Tachycardia who were Administered Amiodarone

2002 ◽  
Vol 17 (6) ◽  
pp. 566-571 ◽  
Author(s):  
Masaya Itoda ◽  
Yoshiro Saito ◽  
Kazuo Komamura ◽  
Kazuyuki Ueno ◽  
Shiro Kamakura ◽  
...  
Keyword(s):  
Ventricular Tachycardia ◽  
Single Nucleotide Polymorphisms ◽  
Japanese Patients ◽  
Nucleotide Polymorphisms ◽  
Single Nucleotide

scholarly journals Identification of Four Novel Synonymous Substitutions in the X-Linked GenesNeuroligin 3andNeuroligin 4Xin Japanese Patients with Autistic Spectrum Disorder

2012 ◽  
Vol 2012 ◽  
pp. 1-5 ◽  
Author(s):  
Kumiko Yanagi ◽  
Tadashi Kaname ◽  
Keiko Wakui ◽  
Ohiko Hashimoto ◽  
Yoshimitsu Fukushima ◽  
...  
Keyword(s):  
Single Nucleotide Polymorphisms ◽  
Mutation Screening ◽  
Melting Curve ◽  
Japanese Patients ◽  
Autism Spectrum ◽  
Ethnic Background ◽  
Spectrum Disorder ◽  
Nucleotide Polymorphisms ◽  
Single Nucleotide ◽  
Synonymous Substitutions

Mutations in the X-linked genesneuroligin 3 (NLGN3)andneuroligin 4X (NLGN4X)were first implicated in the pathogenesis of X-linked autism in Swedish families. However, reports of mutations in these genes in autism spectrum disorder (ASD) patients from various ethnic backgrounds present conflicting results regarding the etiology of ASD, possibly because of genetic heterogeneity and/or differences in their ethnic background. Additional mutation screening study on another ethnic background could help to clarify the relevance of the genes to ASD. We scanned the entire coding regions ofNLGN3andNLGN4Xin 62 Japanese patients with ASD by polymerase chain reaction-high-resolution melting curve and direct sequencing analyses. Four synonymous substitutions, one inNLGN3and three inNLGN4X, were identified in four of the 62 patients. These substitutions were not present in 278 control X-chromosomes from unrelated Japanese individuals and were not registered in the database of Single Nucleotide Polymorphisms build 132 or in the Japanese Single Nucleotide Polymorphisms database, indicating that they were novel and specific to ASD. Though further analysis is necessary to determine the physiological and clinical importance of such substitutions, the possibility of the relevance of both synonymous and nonsynonymous substitutions with the etiology of ASD should be considered.

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