9783384227973 - unveiling the mystery of phenotypic heterogeneity in simplex autism di sharlin (10 risultati)
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Paperback or Softback. Condizione: New. Unveiling the Mystery of Phenotypic Heterogeneity in Simplex Autism. Book.
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Taschenbuch. Condizione: Neu. Unveiling the Mystery of Phenotypic Heterogeneity in Simplex Autism | Sharlin | Taschenbuch | Englisch | 2024 | tredition | EAN 9783384227973 | Verantwortliche Person für die EU: tredition GmbH, Heinz-Beusen-Stieg 5, 22926 Ahrensburg, info[at]tredition[dot]de | Anbieter: preigu.
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Taschenbuch. Condizione: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -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 par…ticularly 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 124 pp. Englisch.
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Kartoniert / Broschiert. Condizione: New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. 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 in…dividuals remains a mystery. This is particularly puzzling in simp.
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Taschenbuch. Condizione: Neu. This item is printed on demand - Print on Demand Titel. Neuware -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 particu…larly 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 approachestredition, Heinz-Beusen-Stieg 5, 22926 Ahrensburg 124 pp. Englisch.
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Taschenbuch. Condizione: Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - 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 particul…arly 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.
