Associated Papers
Identification of novel FATP4 mutations in a Japanese patient with ichthyosis prematurity syndrome.
Tsuge I et al.
Human Genome Variation, 2015
A spontaneous Fatp4/Scl27a4 splice site mutation in a new murine model for congenital ichthyosis.
Tao J et al.
Plos One, 2012
FATP4 missense and nonsense mutations cause similar features in Ichthyosis Prematurity Syndrome.
Sobol M et al.
Bmc Research Notes, 2011
A novel mutation in the fatty acid transport protein 4 gene in a patient initially described as affected by self-healing congenital verruciform hyperkeratosis.
Morice-Picard F et al.
American Journal of Medical Genetics. Part A, 2010
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