Duchenne muscular dystrophy could be treated with genome editing using CRISPR/Cas9 technique

Genome editing using  CRISPR/Cas9 is a promising possibility for correcting diseases due to genetic mutations (see HERE ), such as Duchenne muscular dystrophy – lethal degeneration of cardiac and skeletal muscle caused by different genetic mutations (see more HERE), which...

Genome editing and germ line modification. Medical and ethical debate

Genetic modification of the human germline that will pass to children, and to future Gene editing consists of the modification or removal of specific DNA sequences in order, for example, to correct a disease-causing mutation. Early approaches were based on the recognition of...
Posted On 28 May 2018
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