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Year : 2019 | Volume:  37 | Issue Number:  3 | Page:  150-153

CASE REPORT

Case report of two brothers with a novel homozygous mutation in ALOX12B leads to autosomal recessive congenital ichthyosis: Which type and which subtype? Two siblings with a novel homozygous mutation in ALOX12B
Gumus Evren

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