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Your search keyword '"Chatron N"' showing total 9 results

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9 results on '"Chatron N"'

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1. Progressive Myoclonus Epilepsy Caused by a Homozygous Splicing Variant of SLC7A6OS

3. The epilepsy phenotypic spectrum associated with a recurrent CUX2 variant

7. SOX3 duplication: A genetic cause to investigate in fetuses with neural tube defects.

9. Neonatal tremor episodes and hyperekplexia-like presentation at onset in a child with SCN8A developmental and epileptic encephalopathy.

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