Ectodermal Dysplasia-Skin Fragility Syndrome: A Rare Case Report.

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Ectodermal Dysplasia-Skin Fragility Syndrome: A Rare Case Report.

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2015 nî lūn-bûn

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2015年の論文

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2015年論文

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2015年論文

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2015年論文

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2015年論文

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2015年論文

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Ectodermal Dysplasia-Skin Fragility Syndrome: A Rare Case Report.

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Ectodermal Dysplasia-Skin Fragility Syndrome: A Rare Case Report.

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Ectodermal Dysplasia-Skin Fragility Syndrome: A Rare Case Report.

@en

Ectodermal Dysplasia-Skin Fragility Syndrome: A Rare Case Report.

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Ectodermal Dysplasia-Skin Fragility Syndrome: A Rare Case Report.

@en

Ectodermal Dysplasia-Skin Fragility Syndrome: A Rare Case Report.

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P1476

Ectodermal Dysplasia-Skin Fragility Syndrome: A Rare Case Report.

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P2093

Neelam Sharma

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Subhash Kashyap

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Vinay Shanker

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P2860

Genotype-phenotype correlation in skin fragility-ectodermal dysplasia syndrome resulting from mutations in plakophilin 1

The classification of inherited epidermolysis bullosa (EB): Report of the Third International Consensus Meeting on Diagnosis and Classification of EB

Plakophilin 1: an important stabilizer of desmosomes.

Ectodermal dysplasia-skin fragility syndrome.

Oral rehabilitation of a patient with ectodermal dysplasia with prosthodontics treatment.

Carboxyl terminus of Plakophilin-1 recruits it to plasma membrane, whereas amino terminus recruits desmoplakin and promotes desmosome assembly.

The distribution of the desmosomal protein, plakophilin 1, in human skin and skin tumors.

Ectodermal dysplasia-skin fragility syndrome resulting from a new homozygous mutation, 888delC, in the desmosomal protein plakophilin 1.

Ectodermal dysplasia-skin fragility syndrome.

P304

421

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P31

scholarly article

case report

P356

10.4103/0019-5154.160525

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P407

English

P433

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P577

2015-07-01T00:00:00Z

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P698

26288439

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P932

4533569

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