Comprehensive Genetic Study of a Monozygotic Triplet Discordant for Autism Spectrum Disorder

There are a few comprehensive genetic studies on autism spectrum disorders (ASD) in India. Children of multiple births are valuable for genomics studies of complex disorders such as ASD. We report whole-exome sequencing (WES) in a triplet family in which only one among the triplet has ASD. The objec...

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Veröffentlicht in:	Neurology India 2024-03, Vol.72 (2), p.384-387
Hauptverfasser:	Thanseem, Ismail, Banerjee, Moinak, Melempatt, Nisha, Prakash, Anil, Iype, Mary, Anitha, Ayyappan
Format:	Artikel
Sprache:	eng
Schlagworte:	Autism Spectrum Disorder - genetics Child Exome Sequencing Humans Polymorphism, Single Nucleotide - genetics Triplets - genetics
Online-Zugang:	Volltext
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