Contribution of Whole-Genome Sequencing and Transcript Analysis to Decipher Retinal Diseases Associated with MFSD8 Variants

Publikation

Contribution of Whole-Genome Sequencing and Transcript Analysis to Decipher Retinal Diseases Associated with MFSD8 Variants

Wissenschaftlicher Artikel/Review - 13.04.2022

Poncet Anais F, Smirnov Vasily M, Dollfus Hélène, Defoort-Dhellemmes Sabine, Jobic Florence, Schorderet Daniel F, Devos Aurore, Le Moing Anne-Gaëlle, Todorova Margarita, Bocquet Béatrice, Pelletier Valérie, Drumare Isabelle, Meunier Isabelle, Vaclavik Veronika, Grunewald Olivier, Dhaenens Claire-Marie

Zitation

Poncet A, Smirnov V, Dollfus H, Defoort-Dhellemmes S, Jobic F, Schorderet D, Devos A, Le Moing A, Todorova M, Bocquet B, Pelletier V, Drumare I, Meunier I, Vaclavik V, Grunewald O, Dhaenens C. Contribution of Whole-Genome Sequencing and Transcript Analysis to Decipher Retinal Diseases Associated with MFSD8 Variants. Int J Mol Sci 2022; 23:4294.

Art

Wissenschaftlicher Artikel/Review (Englisch)

Zeitschrift

Int J Mol Sci 2022; 23

Veröffentlichungsdatum

13.04.2022

Seiten

4294