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Pepinmarshall

Pepin Marshall

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This author contributed to 2 pathways:

Dravet syndrome: Scn1a-A1783V point mutation model

Dravet syndrome: Scn1a-A1783V point mutation model

Dravet syndrome

Dravet syndrome

Dravet syndrome: Scn1a-A1783V point mutation model - WP5298 (Mus musculus)
Dravet syndrome - WP5200 (Homo sapiens)

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