Erfan Heidari

Publication Activity (10 Years)

Years Active: 2020-2021
Publications (10 Years): 2

Top Topics

Prefrontal Cortex

Intellectual Disability

Body Mass Index

Top Venues

Annals of human genetics

This page only lists publications with an associated author ORCID identifier.

Publications

Erfan Heidari, Alexander N Harrison, Ehsan Jafarinia, Ali Reza Tavasoli, Navid Almadani, Robert S Molday, Masoud Garshasbi
Novel variants in critical domains of ATP8A2 and expansion of clinical spectrum. Human mutation 42 (5) (2021)
Erfan Heidari, Ehsan Razmara, Sareh Hosseinpour, Ali Reza Tavasoli, Masoud Garshasbi
Homozygous in-frame variant of SCL6A3 causes dopamine transporter deficiency syndrome in a consanguineous family. Annals of human genetics 84 (4) (2020)