Generation of a de novo intronic junction in the DMD gene through CRISPR/Cas genome editing as a potential therapy for a high proportion of Duchenne muscular dystrophy patients.

Monica Rebeca Gil Garzon

Generation of a de novo intronic junction in the DMD gene through CRISPR/Cas genome editing as a potential therapy for a high proportion of Duchenne muscular dystrophy patients.

Monica Rebeca Gil Garzon

Research output: Thesis › Doctoral Thesis

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Original language	English
Qualification	Ph.D.
Awarding Institution	Royal Holloway, University of London
Supervisors/Advisors	Popplewell, Linda, Supervisor Malerba, Alberto, Supervisor
Award date	1 Jan 2024
Publication status	Unpublished - 2023

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2023 Gil Garzon, Monica Rebeca PhD Thesis

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@phdthesis{7029343d236a46cc8a1959522200d5d6,

title = "Generation of a de novo intronic junction in the DMD gene through CRISPR/Cas genome editing as a potential therapy for a high proportion of Duchenne muscular dystrophy patients.",

author = "{Gil Garzon}, {Monica Rebeca}",

year = "2023",

language = "English",

school = "Royal Holloway, University of London",

}