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Genetic Candidate Variants in Two Multigenerational Families with Childhood Apraxia of Speech

Genetic Candidate Variants in Two Multigenerational Families with Childhood Apraxia of Speech

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_plos_journals_1784752450

Genetic Candidate Variants in Two Multigenerational Families with Childhood Apraxia of Speech

About this item

Full title

Genetic Candidate Variants in Two Multigenerational Families with Childhood Apraxia of Speech

Publisher

United States: Public Library of Science

Journal title

PloS one, 2016-04, Vol.11 (4), p.e0153864

Language

English

Formats

Publication information

Publisher

United States: Public Library of Science

More information

Scope and Contents

Contents

Childhood apraxia of speech (CAS) is a severe and socially debilitating form of speech sound disorder with suspected genetic involvement, but the genetic etiology is not yet well understood. Very few known or putative causal genes have been identified to date, e.g., FOXP2 and BCL11A. Building a knowledge base of the genetic etiology of CAS will mak...

Alternative Titles

Full title

Genetic Candidate Variants in Two Multigenerational Families with Childhood Apraxia of Speech

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_plos_journals_1784752450

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_plos_journals_1784752450

Other Identifiers

ISSN

1932-6203

E-ISSN

1932-6203

DOI

10.1371/journal.pone.0153864

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