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    Novel homozygous missense mutation c.1654G>T in the ALOX12B gene causing congenital ichthyosiform erythroderma

    Novel homozygous missense mutation c.1654G>T in the ALOX12B gene causing congenital ichthyosiform erythroderma by Mae, Kotoe, Kawakami, Yoshio, Kajita, Ai, Takeichi, Takuya, Noda, Tatsuhiro, Hirai, Yoji, Akiyama, Masashi, Morizane, Shin

    Published in Journal of dermatology
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