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Clinical and Molecular Aspects of Sjogren-Larsson Syndrome Reported in an Iranian Consanguineous Family with Triplet Affected Individuals
Sjogren-Larsson Skin disease Mutation Iran
2015/9/25
Background: Sjogren Larsson Syndrome (SLS; OMIM: 270200) is an autosomal recessive neuro-cutaneous disorder characterized by mental retardation, congenital ichthyosis and spastic paraplegia. SLS is ca...