Open AccessCase 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
Author(s) -
Evren Gümüş
Publication year - 2019
Publication title -
dermatologica sinica
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.604
H-Index - 17
eISSN - 2223-330X
pISSN - 1027-8117
DOI - 10.4103/ds.ds_35_18
Subject(s) - ichthyosis , congenital ichthyosis , medicine , genetics , mutation , phenotype , dermatology , biology , gene
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