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...

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Detalles Bibliográficos
Autores principales: Justice, Elizabeth D., Barnum, Sarah J., Kidd, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Research Article
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

Internet

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

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