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The WAGR syndrome gene PRRG4 is a functional homologue of the commissureless axon guidance gene
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 func...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Public Library of Science
2017
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5578492/ https://www.ncbi.nlm.nih.gov/pubmed/28859078 http://dx.doi.org/10.1371/journal.pgen.1006865 |