Published in
Springer Nature [academic journals on nature.com], European Journal of Human Genetics, 1(21), p. 82-88, 2012
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12p13.33 microdeletion including ELKS/ERC1, a new locus associated with childhood apraxia of speech
Journal article published in 2012 by
Julien Thevenon 
,
Patrick Callier,
Joris Andrieux,
Bruno Delobel,
Albert David,
Sylvie Sukno,
Delphine Minot,
Laure Mosca Anne,
Nathalie Marle,
Damien Sanlaville,
Marlène Bonnet,
Alice Masurel-Paulet,
Fabienne Levy,
Lorraine Gaunt,
Sandra Farrell
and other authors.
,
Patrick Callier,
Joris Andrieux,
Bruno Delobel,
Albert David,
Sylvie Sukno,
Delphine Minot,
Laure Mosca Anne,
Nathalie Marle,
Damien Sanlaville,
Marlène Bonnet,
Alice Masurel-Paulet,
Fabienne Levy,
Lorraine Gaunt,
Sandra Farrell
and other authors.
This paper is made freely available by the publisher.
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Abstract
Speech sound disorders are heterogeneous conditions, and sporadic and familial cases have been described. However, monogenic inheritance explains only a small proportion of such disorders, in particular in cases with childhood apraxia of speech (CAS). Deletions of