TY - JOUR
T1 - Small intragenic deletion in FOXP2 associated with childhood apraxia of speech and dysarthria
AU - Turner, Samantha J
AU - Hildebrand, Michael S
AU - Block, Susan
AU - Damiano, John
AU - Fahey, Michael Collingwood
AU - Reilly, Sheena
AU - Bahlo, Melanie
AU - Scheffer, Ingrid E
AU - Morgan, Angela Tamsin
PY - 2013
Y1 - 2013
N2 - Relatively little is known about the neurobiological basis of speech disorders although genetic determinants are increasingly recognized. This is the first report of a small intragenic deletion of FOXP2 that is likely to be the cause of severe motor speech disorder associated with language and literacy problems.
AB - Relatively little is known about the neurobiological basis of speech disorders although genetic determinants are increasingly recognized. This is the first report of a small intragenic deletion of FOXP2 that is likely to be the cause of severe motor speech disorder associated with language and literacy problems.
UR - http://onlinelibrary.wiley.com/doi/10.1002/ajmg.a.36055/pdf
UR - https://www.scopus.com/pages/publications/84881666129
U2 - 10.1002/ajmg.a.36055
DO - 10.1002/ajmg.a.36055
M3 - Article
SN - 1552-4825
VL - 161
SP - 2321
EP - 2326
JO - American Journal of Medical Genetics, Part A
JF - American Journal of Medical Genetics, Part A
IS - 9
ER -