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Nature Genetics|August 31, 2001
A Y-encoded subunit of the translation initiation factor Eif2 is essential for mouse spermatogenesisS Mazeyrat, N Saut, V Grigoriev, et al.
Nature Genetics|August 31, 2001
A mutant mitochondrial respiratory chain assembly protein causes complex III deficiency in patients with tubulopathy, encephalopathy and liver failureP de Lonlay, I Valnot, A Barrientos, et al.
Nature Genetics|August 31, 2001
New views on RPE65 deficiency: the rod system is the source of vision in a mouse model of Leber congenital amaurosisM W Seeliger, C Grimm, F Ståhlberg, et al.
Nature Genetics|August 31, 2001
Disruption of an imprinted gene cluster by a targeted chromosomal translocation in miceM A Cleary, C D van Raamsdonk, J Levorse, et al.
Nature Genetics|August 31, 2001
The UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene is mutated in recessive hereditary inclusion body myopathyI Eisenberg, N Avidan, T Potikha, et al.
Nature Genetics|August 31, 2001
Paternal transmission of the very common class I INS VNTR alleles predisposes to childhood obesityC Le Stunff, D Fallin, P Bougnères
Nature Genetics|August 2, 2001
To bind or not to bindM D Biggin
Nature Genetics|August 2, 2001
Mutation of DNASE1 in people with systemic lupus erythematosusK Yasutomo, T Horiuchi, S Kagami, et al.
Nature Genetics|August 2, 2001
IBD sharing around the PPARG locus is not increased in dizygotic twins or their mothersD Duffy, G Montgomery, S Treloar, et al.
Nature Genetics|June 1, 1992
The gene for the peripheral myelin protein PMP-22 is a candidate for Charcot-Marie-Tooth disease type 1AP I Patel, B B Roa, A A Welcher, et al.
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