Suchergebnisse - "Leo, Paul J"

PubPharm (2)

1

Heterozygous loss of WBP11 function causes multiple congenital defects in humans and mice

enthalten in: Human molecular genetics | 2020

von Martin, E. | Enriquez, A. | Sparrow, D. | +31

2

Cross-ethnic meta-analysis identifies association of the GPX3-TNIP1 locus with amyotrophic lateral sclerosis

enthalten in: Nature communications | 2017

von Benyamin, B. | He, J. | Zhao, Q. | +61

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