Functional characterisation of ATP2C2, a gene implicated in language disorders.

Paracchini, Silvia (PI)

Project: Studentship

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2021
A rare missense variant in the ATP2C2 gene is associated with language impairment and related measures
Martinelli, A., Rice, M., Talcott, J. B., Diaz, R., Smith, S., Hashim Raza, M., Snowling, M. J., Hulme, C., Stein, J., Hayiou-Thomas, M. E., Hawi, Z., Kent, L., Pitt, S. J., Newbury, D. F. & Paracchini, S., 15 Jun 2021, In: Human Molecular Genetics. 30, 12, p. 1160–1171 12 p., ddab111.
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