The WAGR syndrome gene PRRG4 is a functional homologue of the commissureless axon guidance gene
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DOI: 10.1371/journal.pgen.1006865
Abstract: WAGR syndrome is characterized by Wilm’s tumor, aniridia, genitourinary abnormalities and intellectual disabilities. WAGR is caused by a chromosomal deletion that includes the PAX6, WT1 and PRRG4 genes. PRRG4 is proposed to contribute to the… read more here.
Keywords: gene; axon guidance; wagr syndrome; prrg4 functional ... See more keywords