Severe neonatal MEGDHEL syndrome with a homozygous truncating mutation in SERAC1

Vineta Fellman*, Rishi Banerjee, Kai-Lan Lin, Ilari Pulli, Helen Cooper, Henna Tyynismaa, Jukka Kallijärvi

*Corresponding author for this work

Research output: Contribution to journal › Article › Scientific › peer-review

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