Mutations in particular genes can cause or increase the risk of specific congenital anomalies of the urogenital system.Which gene when mutated is most likely to be responsible for congenital bilateral aplasia of the vas deferens?

Question

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Mutations in the CFTR (cystic fibrosis transmembrane conductance regulator) gene are known to cause congenital bilateral aplasia of the vas deferens, which is a characteristic feature of cystic fibrosis.

Mutations in Particular Genes Can Cause or Increase the Risk