Molecular analysis of connexin26 asparagine14 mutations associated with syndromic skin phenotypes. [electronic resource]
Producer: 20110916Description: 408-12 p. digitalISSN:- 1600-0625
- Adult
- Asparagine -- genetics
- Aspartic Acid -- genetics
- Cell Membrane -- metabolism
- Child
- Connexin 26
- Connexins -- genetics
- Cytoplasm -- metabolism
- Endoplasmic Reticulum -- metabolism
- Female
- Fluoresceins -- metabolism
- Gap Junctions -- metabolism
- HeLa Cells
- Hearing Loss -- genetics
- Humans
- Hypertrichosis -- genetics
- Keratoderma, Palmoplantar -- drug therapy
- Keratosis -- drug therapy
- Lysine -- genetics
- Male
- Mutation, Missense -- physiology
- Nails, Malformed -- genetics
- Protein Transport -- genetics
- Skin -- pathology
- Skin Diseases -- drug therapy
- Syndrome
- Transfection
- Tyrosine -- genetics
No physical items for this record
Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
There are no comments on this title.
Log in to your account to post a comment.