About the Project
Pulmonary hypertension (PAH) is debilitating condition characterized by thick and stiff blood vessels that are unable to expand resulting in an increased pressure in the blood vessels supplying the lungs. This makes the heart work harder making it weak and can lead to heart failure. Changes in the functioning of some genes increase the risk of PAH. Currently there is no cure for this condition. Moreover, the current treatments are aimed at relieving the symptoms and delivered orally and hence…
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