Associated Papers
Genotype and Clinical Phenotype of Monocarboxylate Transporter 1 Deficiency in Three Palestinian Children: Report of Two Novel Variants in the SLC16A1 Gene.
Dweikat I et al.
American Journal of Medical Genetics. Part A, 2025
Structural heterogeneity of type I collagen triple helix and its role in osteogenesis imperfecta.
Makareeva E et al.
The Journal of Biological Chemistry, 2008
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