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Join date: Mar 9, 2026

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Hsa-let-7a-1 Overexpression Stable Cell Line is engineered for stable overexpression of human miRNA precursor Hsa-let-7a-1.

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You can help find a cure for this rare disease today

Hereditary Spastic Paraplegia (HSP SPG4)  disease is very rare and so there is less incentive for companies to allocate money towards researching the disease and its cure. There is very little funding from the government.  SPG4 is progressive and currently there is no cure to reverse or stop the progression. It is extremely important for affected individuals and their families to help fund the research necessary to help find a cure. With the generosity of selfless donors, we can help Maurya and other deserving children, adults, and their families that have been afflicted by this rare disease.

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