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Showing 2 out of a total of 2 results for community: Atlas of Genetics and Cytogenetics in Oncology and Haematology. (0.002 seconds)
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(ARMGHM - Atlas Génétique des Cancers, 2017)SLC24A5 is a member of the potassium-dependent sodium/calcium exchanger family and encodes an intracellular membrane protein. Sequence variations in this gene have been associated with differences in skin pigmentation, and the defective protein leads to Oculocutaneous albinism type VI, OCA6....
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(ARMGHM - Atlas Génétique des Cancers, 2016)OCA2 gene (OCA2), having a chromosomal location of 15q12-q13, encodes an integral membrane transporter protein playing a role in regulating the pH of melanosomes. OCA2 is hypothesized to be involved in the transport of tyrosine, the precursor to melanin synthesis, within the melanocyte. Defects in this gene are the cause of oculocutaneous albinism type II; OCA II....
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