Suchergebnisse - "Cortón, Marta"

PubPharm (4)

1

Novel genes and sex differences in COVID-19 severity

enthalten in: Human molecular genetics | 2022

von Cruz, R. | Diz-de Almeida, S. | López de Heredia, M. | +101

2

An Alu-mediated duplication in NMNAT1, involved in NAD biosynthesis, causes a novel syndrome, SHILCA, affecting multiple tissues and organs

enthalten in: Human molecular genetics | 2020

von Bedoni, N. | Quinodoz, M. | Pinelli, M. | +17

3

Whole-exome sequencing reveals ZNF408 as a new gene associated with autosomal recessive retinitis pigmentosa with vitreal alterations

enthalten in: Human molecular genetics | 2015

von Avila-Fernandez, A. | Perez-Carro, R. | Corton, M. | +17

4

Whole-exome sequencing reveals ZNF408 as a new gene associated with autosomal recessive retinitis pigmentosa with vitreal alterations

enthalten in: Human molecular genetics | 2015

von Avila-Fernandez, A. | Perez-Carro, R. | Corton, M. | +17

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