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Phenotype expansion of variants affecting p38 MAPK signaling in hypospadias patients
BACKGROUND: Hypospadias is a congenital anomaly of the male urogenital system. Genetics factors play an important role in its pathogenesis. To search for potential causal genes/variants for hypospadias, we performed exome sequencing in a pedigree with three patients across two generations and a coho...
Autores principales: | , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9128137/ https://www.ncbi.nlm.nih.gov/pubmed/35606856 http://dx.doi.org/10.1186/s13023-022-02334-5 |