|  Download for Citation Managers
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
Year : 2019 | Volume: 37 | Issue Number: 3 | Page: 150-153
Click here to read this article
|
| |
|
