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Akhtar and Riffat, 1991)

Sedaghatian-type Spondylometaphyseal Dysplasia (SSMD) Sedaghatian type Spondylometaphyseal Dysplasia (SSMD) is an extremely rare progressive disorder which is characterized by a multi-system presentation, including cupping/flaring of metaphyses, platyspondyly (flattening of the vertebrae), cardiac arrhythmia, and central nervous system (CNS) abnormalities, including hypogenesis of corpus callosum and cerebellar hypoplasia (OMIM #250220) [19]

Tf containing one or two ferric ions binds to transferrin receptor 1 (TfR1), forming a complex that enters the cell via receptor-mediated endocytosis and then enters the non-lysosomal acid compartment

doi:10.3390/nu15061393 32

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Bioorg Med Chem Lett 20:50505053 Innocenti A, ztrk Sarkaya SB, Gulcin I, Supuran CT (2010b) Carbonic anhydrase inhibitors