McMillan, H. J., Worthylake, T., Schwartzentruber, J., Gottlieb, C. C., Lawrence, S. E., MacKenzie, A., . . . Boycott, K. M. (2012). Specific combination of compound heterozygous mutations in 17β-hydroxysteroid dehydrogenase type 4 (HSD17B4) defines a new subtype of D-bifunctional protein deficiency. BioMed Central.
Παραπομπή Chicago StyleMcMillan, Hugh J., et al. Specific Combination of Compound Heterozygous Mutations in 17β-hydroxysteroid Dehydrogenase Type 4 (HSD17B4) Defines a New Subtype of D-bifunctional Protein Deficiency. BioMed Central, 2012.
Παραπομπή MLAMcMillan, Hugh J., et al. Specific Combination of Compound Heterozygous Mutations in 17β-hydroxysteroid Dehydrogenase Type 4 (HSD17B4) Defines a New Subtype of D-bifunctional Protein Deficiency. BioMed Central, 2012.