A case report of de novo missense FOXP1...

Clinical Case Reports 2015 / 02 Vol. 3; Iss. 2

A case report of de novo missense FOXP1 mutation in a non-Caucasian patient with global developmental delay and severe speech impairment

Song, Hao, Makino, Yuka, Noguchi, Emiko, Arinami, Tadao
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Volume:
3
Language:
english
Journal:
Clinical Case Reports
DOI:
10.1002/ccr3.167
Date:
February, 2015
File:
PDF, 58 KB
english, 2015
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