Loss of Gsx1 and Gsx2 function rescues distinct phenotypes in Dlx1/2 mutants.
Wang B; Long JE; Flandin P; Pla R; Waclaw RR; Campbell K; Rubenstein JL; The Journal Of Comparative Neurology, 2013, vol. 521, issue 7, p 1561, ISSN 10969861. ISBN 10969861.

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