PITX2 deficiency and associated human disease: insights from the zebrafish model
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DOI: 10.1093/hmg/ddy074
Abstract: Abstract The PITX2 (paired-like homeodomain 2) gene encodes a bicoid-like homeodomain transcription factor linked with several human disorders. The main associated congenital phenotype is Axenfeld-Rieger syndrome, type 1, an autosomal dominant condition characterized by variable… read more here.
Keywords: associated human; pitx2 deficiency; disease; pitx2 ... See more keywords