Mutational analyses of mitochondrial ATP6 gene reveal a possible association with abnormal levels of lactic acid and ammonia in Bangladeshi children with autism spectrum disorder: A case-control study-Reference-Cited by-同舟云学术

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Mutational analyses of mitochondrial ATP6 gene reveal a possible association with abnormal levels of lactic acid and ammonia in Bangladeshi children with autism spectrum disorder: A case-control study

Published:2024-12 Issue: Volume:42 Page:201325
ISSN:2773-0441
Container-title:Human Gene
language:en
Short-container-title:Human Gene

Author:

Hasan Md. Mahbub,Adiba Maisha,Rahman Molie,Akter Hosneara,Uddin Mohammed,Ebihara Akio,Nabi A.H.M. Nurun,Yasmin Tahirah

Funder

University Grants Commission of Bangladesh

Publisher

Elsevier BV

Reference40 articles.

1. A method and server for predicting damaging missense mutations;Adzhubei;Nat. Methods,2010

2. Renin gene polymorphisms in Bangladeshi hypertensive population;Afruza;Journal of Genomics,2014

3. Prevalence of autism Spectrum disorder (ASD) among the children aged 18-36 months in a rural community of Bangladesh: a cross sectional study [version 1; referees: 1 approved, 2 approved with reservations];Akhter;F1000Research,2018

4. ConSeq: the identification of functionally and structurally important residues in protein sequences;Berezin;Bioinformatics,2004

5. I-Mutant2.0: predicting stability changes upon mutation from the protein sequence or structure;Capriotti;Nucleic Acids Res.,2005

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