Single case links deep intronic MFSD8 variant to CLN7 disease
A single-patient study showed that a deep intronic MFSD8 variant causes CLN7 disease by triggering abnormal pseudoexon inclusion that disrupts ...
A single-patient study showed that a deep intronic MFSD8 variant causes CLN7 disease by triggering abnormal pseudoexon inclusion that disrupts ...
© 2025 Scienmag - Science Magazine
© 2025 Scienmag - Science Magazine