Novel homozygous FRRS1L variant reported in Chinese girl with DEE37-related symptoms
A single-patient case report documents a novel homozygous FRRS1L variant in a Chinese girl with developmental delay, epilepsy, movement abnormalities, ...
A single-patient case report documents a novel homozygous FRRS1L variant in a Chinese girl with developmental delay, epilepsy, movement abnormalities, ...
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