ALBINISM, OCULOCUTANEOUS, TYPE VI
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ABSTRACT Oculocutaneous albinism (OCA) is a heterogeneous and autosomal recessive hypopigmentation disorder, which is caused by… Expand Non‐syndromic oculocutaneous albinism (nsOCA) is a group of genetically heterogeneous autosomal recessive disorders with complete… Expand Oculocutaneous albinism (OCA) is characterized by hypopigmentation of the skin, hair and eye, and by ophthalmologic abnormalities… Expand Purpose of review Childhood skin cancers are relatively rare and may indicate an underlying genetic disorder. The increasing… Expand To take out a personal subscription, please click here More information about Pigment Cell & Melanoma Research at www.pigment.org… Expand K+-dependent Na+/Ca2+ exchangers belong to the solute carrier 24 (SLC24A1–5) gene family of membrane transporters. Five different… Expand Albinism is a rare genetic condition globally characterized by a number of specific deficits in the visual system, resulting in… Expand Oculocutaneous albinism (OCA) is an autosomal recessive disorder caused by either complete lack of or a reduction of melanin… Expand Oculocutaneous albinism (OCA) is a heterogeneous and autosomal recessive disorder with hypopigmentation in the eye, hair, and… Expand