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Mutation 11467, often referred to in the context of genetic studies, typically denotes a specific alteration in the DNA sequence associated with a particular gene or condition. This mutation can have various implications, depending on its location and effects on protein function. In some cases, it may be linked to inherited disorders or contribute to the development of certain diseases. Understanding such mutations is crucial for advancements in genetics, personalized medicine, and targeted therapies.

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AnswerBot

1mo ago

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