[HTML][HTML] Analysis of KRT5 and KRT14 gene mutations and mode of inheritance in Iranian patients with clinical suspicion of Epidermolysis bullosa simplex
P Khani, SF Forghani, ZA Kachoei… - Medical Journal of the …, 2020 - ncbi.nlm.nih.gov
Background: Epidermolysis bullosa simplex is a hereditary skin disorder caused by
mutations in several genes such as KRT5 and KRT14. Skin fragility in basal keratinocytes …
mutations in several genes such as KRT5 and KRT14. Skin fragility in basal keratinocytes …
[PDF][PDF] Analysis of KRT5 and KRT14 gene mutations and mode of inheritance in Iranian patients with clinical suspicion of Epidermolysis bullosa simplex
P Khani, SF Forghani, ZA Kachoei, A Zekri… - Med J Islam Repub …, 1934 - academia.edu
Background: Epidermolysis bullosa simplex is a hereditary skin disorder caused by
mutations in several genes such as KRT5 and KRT14. Skin fragility in basal keratinocytes …
mutations in several genes such as KRT5 and KRT14. Skin fragility in basal keratinocytes …
Analysis of KRT5 and KRT14 gene mutations and mode of inheritance in Iranian patients with clinical suspicion of Epidermolysis bullosa simplex.
P Khani, F Forghani, A Zekri, F Ghazi - Medical Journal of the …, 2020 - europepmc.org
Background: Epidermolysis bullosa simplex is a hereditary skin disorder caused by
mutations in several genes such as KRT5 and KRT14. Skin fragility in basal keratinocytes …
mutations in several genes such as KRT5 and KRT14. Skin fragility in basal keratinocytes …
Analysis of KRT5 and KRT14 gene mutations and mode of inheritance in Iranian patients with clinical suspicion of Epidermolysis bullosa simplex
P Khani, SF Forghani, ZA Kachoei… - Medical journal of …, 2020 - pubmed.ncbi.nlm.nih.gov
Background: Epidermolysis bullosa simplex is a hereditary skin disorder caused by
mutations in several genes such as KRT5 and KRT14. Skin fragility in basal keratinocytes …
mutations in several genes such as KRT5 and KRT14. Skin fragility in basal keratinocytes …
[PDF][PDF] Analysis of KRT5 and KRT14 gene mutations and mode of inheritance in Iranian patients with clinical suspicion of Epidermolysis bullosa simplex
P Khani, SF Forghani, ZA Kachoei, A Zekri, F Ghazi - sid.ir
Background: Epidermolysis bullosa simplex is a hereditary skin disorder caused by
mutations in several genes such as KRT5 and KRT14. Skin fragility in basal keratinocytes …
mutations in several genes such as KRT5 and KRT14. Skin fragility in basal keratinocytes …
[PDF][PDF] Analysis of KRT5 and KRT14 gene mutations and mode of inheritance in Iranian patients with clinical suspicion of Epidermolysis bullosa simplex
P Khani, SF Forghani, ZA Kachoei, A Zekri… - Med J Islam Repub …, 1934 - scholar.archive.org
Background: Epidermolysis bullosa simplex is a hereditary skin disorder caused by
mutations in several genes such as KRT5 and KRT14. Skin fragility in basal keratinocytes …
mutations in several genes such as KRT5 and KRT14. Skin fragility in basal keratinocytes …
[PDF][PDF] Analysis of KRT5 and KRT14 gene mutations and mode of inheritance in Iranian patients with clinical suspicion of Epidermolysis bullosa simplex
P Khani, SF Forghani, ZA Kachoei, A Zekri, F Ghazi - sid.ir
Background: Epidermolysis bullosa simplex is a hereditary skin disorder caused by
mutations in several genes such as KRT5 and KRT14. Skin fragility in basal keratinocytes …
mutations in several genes such as KRT5 and KRT14. Skin fragility in basal keratinocytes …