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PTEN Patient Registry and Natural History Study is sponsored by PTEN Foundation. This patient-powered registry and natural history study for the PTEN Hamartoma Tumor Syndrome (PHTS) community aims to engage patients in data-sharing to accelerate research and drug development. It collects uniform data to characterize the patient population, facilitate best practices, and provide information on ongoing research and clinical trials.
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Or search similar grants →According to the current listing, eligibility includes: Individuals who have a PTEN Hamartoma Tumor Syndrome (PHTS) diagnosis, or their guardians/caregivers. Confirm the full requirements in the official notice before applying.
PTEN Patient Registry and Natural History Study is funded by PTEN Foundation. Verify program details on the funder's official page before applying.
Start from the official opportunity page linked in this listing — it carries the sponsor's submission instructions.
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