Erfan Heidari
2PUBLICATIONS
3CO-AUTHORS
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Publications (2)
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|Feb 10, 2021
Novel variants in critical domains of ATP8A2 and expansion of clinical spectrum.Erfan Heidari, Alexander N Harrison, Ehsan Jafarinia
|Feb 21, 2020
Homozygous in-frame variant of SCL6A3 causes dopamine transporter deficiency syndrome in a consanguineous family.Erfan Heidari, Ehsan Razmara, Sareh Hosseinpour
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