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Diagnosis of Pompe disease is sometimes challenging because it exhibits clinical similarities to muscular dystrophy.We describe a case of Becker muscular dystrophy (BMD) with a remarkable reduction in activity of the acid α-glucosidase (GAA) enzyme, caused by a combination of pathogenic mutation and polymorphism variants resulting in pseudodeficiency in GAA. The three-year-old boy demonstrated asymptomatic...
Colored organic anions such as tetra(4-carboxyphenyl)porphyrin (TPP-C), tetra(4-sulfonatophenyl)porphyrin (TPP-S), tetracarboxyphthalocyaninato cobalt (TPC-C) and others were intercalated into the Mg/Al and Zn/Al layered double hydroxides (LDHs). After the intercalation of organic anions, interlayer spacing of the LDHs increased to 7.8-30.7 depending on the amounts of intercalated anions and the...
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