Become a Readings Member to make your shopping experience even easier. Sign in or sign up for free!

Become a Readings Member. Sign in or sign up for free!

Unveiling the Mystery of Phenotypic Heterogeneity in Simplex Autism
Paperback

Unveiling the Mystery of Phenotypic Heterogeneity in Simplex Autism

$63.99
Sign in or become a Readings Member to add this title to your wishlist.

Autism Spectrum Disorder (ASD) presents a complex puzzle. While recent genetic advances have identified genes linked to ASD, the vast variation in symptoms (phenotypic heterogeneity) among individuals remains a mystery. This is particularly puzzling in simplex autism, where only one child in a family is affected. Despite a seemingly simpler genetic background, these cases still display a surprising range of symptoms. This work delves into this very mystery. By analyzing genetic data and phenotypic traits in simplex autism cohorts, researchers aim to uncover the link between specific gene mutations and the severity of ASD symptoms. This in-depth exploration has the potential to shed light on why individuals with similar genetic mutations can exhibit such diverse characteristics. The findings could pave the way for a deeper understanding of the underlying causes of ASD heterogeneity and ultimately lead to more personalized treatment approaches

In Shop
Out of stock
Shipping & Delivery

$9.00 standard shipping within Australia
FREE standard shipping within Australia for orders over $100.00
Express & International shipping calculated at checkout

MORE INFO
Format
Paperback
Publisher
Tredition Gmbh
Date
14 May 2024
Pages
126
ISBN
9783384227973

Autism Spectrum Disorder (ASD) presents a complex puzzle. While recent genetic advances have identified genes linked to ASD, the vast variation in symptoms (phenotypic heterogeneity) among individuals remains a mystery. This is particularly puzzling in simplex autism, where only one child in a family is affected. Despite a seemingly simpler genetic background, these cases still display a surprising range of symptoms. This work delves into this very mystery. By analyzing genetic data and phenotypic traits in simplex autism cohorts, researchers aim to uncover the link between specific gene mutations and the severity of ASD symptoms. This in-depth exploration has the potential to shed light on why individuals with similar genetic mutations can exhibit such diverse characteristics. The findings could pave the way for a deeper understanding of the underlying causes of ASD heterogeneity and ultimately lead to more personalized treatment approaches

Format
Paperback
Publisher
Tredition Gmbh
Date
14 May 2024
Pages
126
ISBN
9783384227973