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Myotonic Dystrophy Type 1 DMK gene Contact details: Bristol Genetics Laboratory South mead Hospital Bristol, BS10 5NB Inquiries: 0117 414 6168 FAX: 0117 414 6464Clinical Background and Genetics Head
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Myotonic dystrophy type 1 is a genetic disorder that affects muscle function and can cause a variety of symptoms.
Individuals who have been diagnosed with myotonic dystrophy type 1 may be required to file relevant paperwork for medical and insurance purposes.
To fill out myotonic dystrophy type 1 paperwork, individuals will need to provide medical history, test results, and other relevant information.
The purpose of myotonic dystrophy type 1 paperwork is to document and track the progress of the disease in affected individuals.
Information such as symptoms, genetic testing results, and treatment plans must be reported on myotonic dystrophy type 1 paperwork.
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