A novel mutation in Keratin 10 passed down in a family with familial steatocystoma multiplex
Saved in:
Main Authors: | Kun-Lin Lu (Author), Chuang-Wei Wang (Author), Wen-Hung Chung (Author), Fang-Ying Wang (Author) |
---|---|
Format: | Book |
Published: |
Wolters Kluwer Medknow Publications,
2022-01-01T00:00:00Z.
|
Subjects: | |
Online Access: | Connect to this object online. |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Acral steatocystoma multiplex
by: Manjula Jain, et al.
Published: (2013) -
Steatocystoma multiplex masquerading as neurofibromas
by: Neha Chandrakumar Bhatt, et al.
Published: (2014) -
Steatocystoma multiplex: A review
by: Manahel Mahmood AlSabbagh
Published: (2016) -
Steatocystoma multiplex limited to the forearms
by: Yasser Alqubaisy, et al.
Published: (2016) -
ER: Yag laser therapy for steatocystoma multiplex
by: Mumcuoglu Ceyda, et al.
Published: (2010)