Epidermolysis bullosa with congenital absence of skin: Clinical and genetic characterization of a 23‐case series-Reference-Cited by-同舟云学术

Epidermolysis bullosa with congenital absence of skin: Clinical and genetic characterization of a 23‐case series

Author:

Mariath Luiza M.¹^ORCID,Santin Juliana T.²,Frantz Jeanine A.³,Doriqui Maria J.R.⁴,Schuler‐Faccini Lavínia¹⁵^ORCID,Kiszewski Ana E.⁶⁷^ORCID

Affiliation:

1. Postgraduate Program in Genetics and Molecular Biology Universidade Federal do Rio Grande do Sul Porto Alegre Brazil

2. Postgraduate Program in Child and Adolescent Health Universidade Federal do Rio Grande do Sul Porto Alegre Brazil

3. DEBRA Brasil Blumenau Brazil

4. Section of Medical Genetics Hospital Infantil Dr. Juvêncio Mattos São Luís Brazil

5. Instituto Nacional de Ciência e Tecnologia de Genética Médica Populacional (INaGeMP) Porto Alegre Brazil

6. Section of Dermatology Universidade Federal de Ciências da Saúde de Porto Alegre Porto Alegre Brazil

7. Section of Pediatric Dermatology Hospital da Criança Santo Antônio, Irmandade da Santa Casa de Misericórdia de Porto Alegre Porto Alegre Brazil

Funder

Instituto Nacional de Ciência e Tecnologia de Genética Médica Populacional

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

Reference5 articles.

3. Consensus re‐classification of inherited epidermolysis bullosa and other disorders with skin fragility;Has C;Br J Dermatol,2020

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