Erratum: Loss of Gsx1 and Gsx2 function rescues distinct phenotypes in Dlx1/2 mutants (J Comp Neurol., (2013), 21, 7, (1561-84), 10.1002/cne.23242);Loss of Gsx1 and Gsx2 function rescues distinct phenotypes in Dlx1/2 mutants

Journal of Comparative Neurology

Volumn 521, Issue 7, 2013, Pages 1561-1584

  Wang, Bei ^a,c   Long, Jason E ^a,c   Flandin, Pierre ^a,d   Pla, Ramon ^a   Waclaw, Ronald R ^b   Campbell, Kenneth ^b   Rubenstein, John L R ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b UNIVERSITY OF CINCINNATI COLLEGE OF MEDICINE   (United States)

^c GENENTECH INC   (United States)

^d Quanticel Pharmaceuticals   (United States)

Author keywords

Basal ganglia; CGE; Development; Dlx; GABA; Gsx; Interneuron; LGE; MGE; Mutant; Septum

Indexed keywords

GLUTAMATE DECARBOXYLASE; GLUTAMIC ACID DECARBOXYLASE 1; OLIGODENDROCYTE TRANSCRIPTION FACTOR 2; TRANSCRIPTION FACTOR HES 5; TRANSCRIPTION FACTOR MASH1; UNCLASSIFIED DRUG;

ANIMAL TISSUE; ARTICLE; ASCL1 GENE; BRAIN DEVELOPMENT; CAUDAL GANGLIONIC EMINENCE; CONTROLLED STUDY; DLX1 GENE; DLX2 GENE; EMBRYO; GANGLION; GENE; GENE EXPRESSION; GENE INTERACTION; GSX1 GENE; GSX2 GENE; HES5 GENE; LATERAL GANGLIONIC EMINENCE; LOSS OF FUNCTION MUTATION; MEDIAL GANGLIONIC EMINENCE; MORPHOGENESIS; MOUSE; MUTANT; NERVE CELL DIFFERENTIATION; NONHUMAN; OLIG2 GENE; PHENOTYPE; PRIORITY JOURNAL; PROTEIN EXPRESSION; SEPTUM PELLUCIDUM;

EID: 84875302751     PISSN: 00219967     EISSN: 10969861     Source Type: Journal    
DOI: 10.1002/cne.25592     Document Type: Erratum

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