Inactivating WRN Gene Mutation

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A change in the nucleotide sequence of the WRN gene that either inhibits expression or results in the translation of an inactive Werner syndrome ATP-dependent helicase protein.

**Synonyms:** - Inactivating RECQ3 Gene Mutation - Inactivating RECQL2 Gene Mutation - Inactivating RECQL3 Gene Mutation - Inactivating WRN Mutation - Inactivating Werner Syndrome Gene Mutation - WRN Gene Inactivation - WRN Inactivating Gene Mutation - WRN Inactivating Mutation - WRN Loss of Function Gene Mutation - WRN Loss of Function Mutation