Allele-Specific Inactivation of an Autosomal Dominant Epidermolysis Bullosa Simplex Mutation Using CRISPR-Cas9-Reference-Cited by-同舟云学术

Allele-Specific Inactivation of an Autosomal Dominant Epidermolysis Bullosa Simplex Mutation Using CRISPR-Cas9

Published:2022-08-01 Issue:4 Volume:5 Page:586-597
ISSN:2573-1599
Container-title:The CRISPR Journal
language:en
Short-container-title:The CRISPR Journal

Author:

Bchetnia Mbarka¹²,Dionne Gagné Rebecca¹,Powell Julie³,Morin Charles⁴,McCuaig Catherine³,Dupérée Audrey⁴,Germain Lucie⁵⁶,Tremblay Jacques P.⁶,Laprise Catherine¹²^ORCID

Affiliation:

1. Département des Sciences Fondamentales and Université Laval, Québec, Canada.

2. Centre intersectoriel en santé durable (CISD), Université du Québec à Chicoutimi (UQAC), Saguenay, Canada; Université Laval, Québec, Canada.

3. Service de Dermatologie, CHU Sainte-Justine, Montréal, Canada; Université Laval, Québec, Canada.

4. Centre Intégré Universitaire de Santé et de Services Sociaux du Saguenay-Lac-Saint-Jean, Hôpital Universitaire de Chicoutimi, Saguenay, Canada; and Université Laval, Québec, Canada.

5. Département de chirurgie, Faculté de médecine, Centre de Recherche en Organogénèse Expérimentale de l'Université Laval/LOEX, and Université Laval, Québec, Canada.

6. Centre de recherche du CHU de Québec, Université Laval, Québec, Canada.

Publisher

Mary Ann Liebert Inc

Subject

Genetics,Biotechnology

Link

https://www.liebertpub.com/doi/pdf/10.1089/crispr.2021.0132

Reference50 articles.

1. Epidermolysis Bullosa Simplex

2. Inherited epidermolysis bullosa: Updated recommendations on diagnosis and classification

3. Revised clinical and laboratory criteria for subtypes of inherited epidermolysis bullosa

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