Suchergebnisse - "Ahimaz, Priyanka"

PubPharm (3)

1

Bi-allelic missense disease-causing variants in RPL3L associate neonatal dilated cardiomyopathy with muscle-specific ribosome biogenesis

enthalten in: Human genetics | 2020

von Ganapathi, M. | Argyriou, L. | Martínez-Azorín, F. | +21

2

Examining the Psychosocial Impact of Genetic Testing for Cardiomyopathies

enthalten in: Journal of genetic counseling | 2017

von Wynn, J. | Holland, D. | Duong, J. | +2

3

Disruption of the ATXN1-CIC complex causes a spectrum of neurobehavioral phenotypes in mice and humans

enthalten in: Nature genetics | 2017

von Lu, H. | Tan, Q. | Rousseaux, M. | +34

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