Kindler syndrome: A rare case report
Kindler syndrome is a very rare genodermatosis with an autosomal recessive pattern and about 250 cases have been reported worldwide. The mutant gene is Fermitin family homolog 1 gene (KIND1), located on chromosome 20p12.3, which encodes for focal adhesion protein "Fermitin family homologue 1 pr...
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Wolters Kluwer Medknow Publications,
2021-01-01T00:00:00Z.
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