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Epileptic Disorders; February 2024, Vol. 26 Issue: 1 p60-68, 9p
In Clinical Neurophysiology Practice 2020 5:142-146
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American Journal of Medical Genetics. Part A; Jul2021, Vol. 185 Issue 7, p2164-2167, 4p
Adult phenotype of the homozygous missense mutation c.655G>A, p.Gly219Arg in SLC13A5: A case report.
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American Journal of Medical Genetics. Part A; Nov2020, Vol. 182 Issue 11, p2671-2674, 4p
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American Journal of Medical Genetics. Part A; Dec2019, Vol. 179 Issue 12, p2481-2485, 5p
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Hynynen, Johanna; Pokka, Tytti; Komulainen‐Ebrahim, Jonna; Myllynen, Päivi; Kärppä, Mikko; Pylvänen, Laura; Kälviäinen, Reetta; Sokka, Arja; Jyrkilä, Aino; Lähdetie, Jaana; Haataja, Leena; Mäkitalo, Anna; Ylikotila, Pauli; Eriksson, Kai; Haapala, Piia; Ansakorpi, Hanna; Hinttala, Reetta; Vieira, Päivi; Majamaa, Kari; Rantala, Heikki
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[AR] Lähdetie, Jaana
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