A novel mutation in the fatty acid transport protein 4 gene in a patient initially described as affected by self-healing congenital verruciform hyperkeratosis. [electronic resource]
- American journal of medical genetics. Part A Oct 2010
- 2664-5 p. digital
Publication Type: Letter
1552-4833
10.1002/ajmg.a.33648 doi
Child Fatty Acid Transport Proteins--genetics Humans Hyperkeratosis, Epidermolytic--genetics Infant, Newborn Infant, Premature Male Mutation Mutation, Missense Remission, Spontaneous