Homozygous Deletion Mutation of the FERMT1 Gene in a Chinese Patient with Kindler Syndrome.
- Author:
Seung Joon OH
1
;
Song Ee KIM
;
Sang Eun LEE
;
Soo Chan KIM
Author Information
- Publication Type:Brief Communication
- MeSH: Asian Continental Ancestry Group*; Humans; Sequence Deletion*
- From:Annals of Dermatology 2016;28(4):503-505
- CountryRepublic of Korea
- Language:English
- Abstract: No abstract available.
