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Biallelic loss of function variants in ATP1A2 cause hydrops fetalis, microcephaly, arthrogryposis and extensive cortical malformations. [electronic resource] by
- Monteiro, Fabiola P
- Curry, Cynthia J
- Hevner, Robert
- Elliott, Stephen
- Fisher, Jamie H
- Turocy, John
- Dobyns, William B
- Costa, Larissa A
- Freitas, Erika
- Kitajima, João Paulo
- Kok, Fernando
Producer: 20200930
In:
European journal of medical genetics vol. 63
Availability: No items available.
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