Sjögren-Larsson syndrome: novel mutations in the ALDH3A2 gene in a French cohort.

Sarret, Catherine

Sjögren-Larsson syndrome: novel mutations in the ALDH3A2 gene in a French cohort. [electronic resource] - Journal of the neurological sciences Jan 2012 - 123-6 p. digital

Publication Type: Journal Article

1878-5883

10.1016/j.jns.2011.08.006 doi


Adolescent
Aldehyde Oxidoreductases--genetics
Child
Cohort Studies
Female
France
Humans
Infant
Male
Point Mutation--genetics
Radiography
Sjogren-Larsson Syndrome--diagnostic imaging