ﺑﺎﺯﮔﺸﺖ ﺑﻪ ﺻﻔﺤﻪ ﻗﺒﻠﯽ
خرید پکیج
تعداد آیتم قابل مشاهده باقیمانده : -20 مورد

Oculocutaneous albinism type 1B

Oculocutaneous albinism type 1B
A patient with oculocutaneous albinism type 1B (OCA1B), due to two mutations in the TYR gene, was born with white hair and lashes but, later in childhood, developed some pigment.
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