|
Year : 2019 |
Volume: 37 |
Issue Number: 3
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
|
| No one has added comments on this article. Click here to add your remarks |
|
Reader
Comments