[HTML][HTML] A Novel Mutation p. L461P in KRT5 Causing Localized Epidermolysis Bullosa Simplex
X Jiang, Y Zhu, H Sun, F Gu - Annals of Dermatology, 2021 - ncbi.nlm.nih.gov
Background Epidermolysis bullosa (EB) is a rare genetic disease with widely different
clinical manifestations, but the relationship between genotype and phenotype is not fully …
clinical manifestations, but the relationship between genotype and phenotype is not fully …
A Novel Mutation p. L461P in KRT5 Causing Localized Epidermolysis Bullosa Simplex
X Jiang, Y Zhu, H Sun, F Gu - Ann Dermatol Vol, 2021 - papersearch.net
Background: Epidermolysis bullosa (EB) is a rare genetic disease with widely different
clinical manifestations, but the relationship between genotype and phenotype is not fully …
clinical manifestations, but the relationship between genotype and phenotype is not fully …
A Novel Mutation p.L461P in KRT5 Causing Localized Epidermolysis Bullosa Simplex.
X Jiang, Y Zhu, H Sun, F Gu - Annals of Dermatology, 2020 - europepmc.org
Background Epidermolysis bullosa (EB) is a rare genetic disease with widely different
clinical manifestations, but the relationship between genotype and phenotype is not fully …
clinical manifestations, but the relationship between genotype and phenotype is not fully …
[引用][C] 1. A Novel Mutation p. L461P inKRT5Causing Localized Epidermolysis Bullosa Simplex
X Jiang - spandidos-publications.com
A Novel Mutation p. L461P in KRT5 Causing Localized Epidermolysis Bullosa Simplex
X JIANG, Y ZHU, H SUN, F GU - Annals of Dermatology, 2021 - pesquisa.bvsalud.org
Background@# Epidermolysis bullosa (EB) is a rare genetic disease with widely different
clinical manifestations, but the relationship between genotype and phenotype is not fully …
clinical manifestations, but the relationship between genotype and phenotype is not fully …
A Novel Mutation p. L461P in KRT5 Causing Localized Epidermolysis Bullosa Simplex
X Jiang, Y Zhu, H Sun, F Gu - Annals of dermatology, 2021 - pubmed.ncbi.nlm.nih.gov
Background Epidermolysis bullosa (EB) is a rare genetic disease with widely different
clinical manifestations, but the relationship between genotype and phenotype is not fully …
clinical manifestations, but the relationship between genotype and phenotype is not fully …
A Novel Mutation p. L461P in KRT5 Causing Localized Epidermolysis Bullosa Simplex
X Jiang, H Sun - Annals of Dermatology, 2021 - kiss.kstudy.com
Background: Epidermolysis bullosa (EB) is a rare genetic disease with widely different
clinical manifestations, but the relationship between genotype and phenotype is not fully …
clinical manifestations, but the relationship between genotype and phenotype is not fully …
A Novel Mutation p. L461P in KRT5 Causing Localized Epidermolysis Bullosa Simplex
J Xin, Z Yingyu, S Huihui, G Feng - Annals of Dermatology, 2021 - dbpia.co.kr
Background: Epidermolysis bullosa (EB) is a rare genetic disease with widely different
clinical manifestations, but the relationship between genotype and phenotype is not fully …
clinical manifestations, but the relationship between genotype and phenotype is not fully …
[HTML][HTML] A Novel Mutation p. L461P in KRT5 Causing Localized Epidermolysis Bullosa Simplex
X Jiang, Y Zhu, H Sun, F Gu - Annals of Dermatology, 2021 - anndermatol.org
Background Epidermolysis bullosa (EB) is a rare genetic disease with widely different
clinical manifestations, but the relationship between genotype and phenotype is not fully …
clinical manifestations, but the relationship between genotype and phenotype is not fully …
A Novel Mutation p. L461P in KRT5 Causing Localized Epidermolysis Bullosa Simplex
X Jiang, H Sun - Annals of Dermatology, 2021 - kiss.kstudy.com
Background: Epidermolysis bullosa (EB) is a rare genetic disease with widely different
clinical manifestations, but the relationship between genotype and phenotype is not fully …
clinical manifestations, but the relationship between genotype and phenotype is not fully …