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5CO-AUTHORS

Developmental genetics (incl. sex determination)

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|Apr 26, 2024

Discovery of a novel homozygous SOD1 truncating variant bolsters infantile SOD1 deficiency syndrome.

Mustafa Dogan, Kerem Teralı, Recep Eroz

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Mustafa Dogan

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Kerem Teralı

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Recep Eroz

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Alper Gezdirici

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Mustafa Dogan

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Kerem Teralı

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Recep Eroz

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