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Genetic insights into Tietz albinism‐deafness syndrome: A new dominant‐negative mutation in MITF.
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- المؤلفون: Yamamoto, Kohei1 (AUTHOR); Okamura, Ken1 (AUTHOR) k‐‐u.ac.jp; Wakamatsu, Kazumasa2 (AUTHOR); Ito, Shosuke2 (AUTHOR); Akabane, Kozue3 (AUTHOR); Arai, Yosuke1 (AUTHOR); Kawaguchi, Junnosuke1 (AUTHOR); Hozumi, Yutaka1 (AUTHOR); Suzuki, Tamio1 (AUTHOR)
- المصدر:
Pigment Cell & Melanoma Research. Jul2024, Vol. 37 Issue 4, p430-437. 8p.
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