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[18] [19] Clinical significance [edit] A mutation in the tyrosinase gene resulting in impaired tyrosinase production leads to type I oculocutaneous albinism, a hereditary disorder that affects one in every 20,000 people

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Inject slowly over 510 seconds to minimize injection site pain

Targeting B7-H3 via chimeric antigen receptor T cells and bispecific killer cell engagers augments antitumor response of cytotoxic lymphocytes

doi: 10.1111/ijpo.12177 194 HorikawaYEnyaMKomagataMHashimotoKIKagamiMFukamiMet al