Beer, N., Osbak, K., van de Bunt, M., Tribble, N., Steele, A., Wensley, K., . . . Gloyn, A. (2012). Insights into the pathogenicity of rare missense GCK variants from the identification and functional characterization of compound heterozygous and double mutations inherited in cis.
Chicago Style (17. basım) AtıfBeer, N., et al. Insights into the Pathogenicity of Rare Missense GCK Variants from the Identification and Functional Characterization of Compound Heterozygous and Double Mutations Inherited in Cis. 2012.
MLA (9th ed.) AtıfBeer, N., et al. Insights into the Pathogenicity of Rare Missense GCK Variants from the Identification and Functional Characterization of Compound Heterozygous and Double Mutations Inherited in Cis. 2012.
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