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Description
Molecular Biology of Primary Carnitine Deficiency The SLC22A5 (OCTN2) gene is located on chromosome 5q31.1 and is composed of 11 exons that generate two alternatively spliced mRNAs encoding proteins of 581 amino acids (isoform a) and 557 amino acids (isoform b)

Therefore, AF can differentiate its pattern types and susceptibility factors according to its physical constitution to take preventive and curative measures as early as possible, which reflects the concept of holism of TCM as well as the pattern differentiation and treatment

doi:10.1016/0092-8674(84)90015-1

Recombinant human thioredoxin ameliorates imiquimodinduced psoriasislike dermatitis in mice

Nat Chem Biol 2013

Soc , 36, 64A Hassan, F
