The WAGR syndrome gene PRRG4 is a functional homologue of the commissureless axon guidance gene
The WAGR syndrome gene PRRG4 is a functional homologue of the commissureless axon guidance gene
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United States: Public Library of Science
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English
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United States: Public Library of Science
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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 autistic symptoms of WAGR syndrome, but the molecular function of PRRG4 genes remains unknown. The Drosophil...
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The WAGR syndrome gene PRRG4 is a functional homologue of the commissureless axon guidance gene
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TN_cdi_plos_journals_1939435840
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https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_plos_journals_1939435840
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1553-7404,1553-7390
E-ISSN
1553-7404
DOI
10.1371/journal.pgen.1006865
