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 protein...
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| Asıl Yazarlar: | , , |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Wolters Kluwer Medknow Publications
2021-01-01
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| Seri Bilgileri: | Muller Journal of Medical Sciences and Research |
| Konular: | |
| Online Erişim: | http://www.mjmsr.net/article.asp?issn=0975-9727;year=2021;volume=12;issue=1;spage=52;epage=55;aulast=Kandikatla |
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