Case Report: Sjogren-Larsson Syndrome: Two Cases from One Family
Sjogren-Larsson Syndrome (SLS) is an autosomal recessive disorder characterized by generalized Ichthyosis, mental retardation, spastic diplegia or tetraplegia and epilepsy. This is a rare syndrome that caused by mutation in the ALDH3A2 gene, on chromosome 17p11.2. That encodes fatty aldehyde dehydro...
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| Format: | Book |
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University of Social Welfare and Rehabilitation Sciences,
2006-04-01T00:00:00Z.
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A1234.567 |
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