Oculocutaneous albinism type 1 (OCA1) results from mutations in the tyrosinase gene, which lead to partial or complete loss of activity of the corresponding enzyme. A large number of mutations have ...
We were unable to process your request. Please try again later. If you continue to have this issue please contact customerservice@slackinc.com. A 14-year-old male presented for his annual eye ...
Researchers at the National Eye Institute (NEI) have developed the first patient-derived stem cell model for studying eye conditions related to oculocutaneous albinism (OCA). The model's development ...
Researchers have developed the first patient-derived stem cell model for studying eye conditions related to oculocutaneous albinism (OCA). The model's development is described in the January issue of ...
606933 (TYR), protein: Tyrosinase. RefSeq: NG_008748.1. Transcript: NM_000372.4 611409 (OCA2), protein: OCA2. RefSeq: NG_009846.1. Transcript: NM_000275.2 115501 ...
The model’s development is described in the January issue of the journal Stem Cell Reports. NEI is part of the National Institutes of Health. “This ‘disease-in-a-dish’ system will help us understand ...
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