Deficiency Of Pyrroline-5-carboxylate Reductase

Overview of Deficiency Of Pyrroline-5-carboxylate Reductase

Most recent studies have shown that Deficiency Of Pyrroline-5-carboxylate Reductase shares some biological mechanisms with avitaminosis, disease-of-adrenal-medulla, epilepsy, epilepsy-pyridoxine-dependent, hereditary-diseases, homocystinuria, hyperlipidemia, hypophosphatasia, inborn-errors-of-metabolism, memory-disorders, memory-impairment, metabolic-diseases, mutation-out-of-frame, neurodegenerative-disorders, nonketotic-hyperglycinemia, proline-dehydrogenase-deficiency, vitamin-b-6-deficiency.

Among the many pathways, these few ones have gauged particular interests from scientists studying Deficiency Of Pyrroline-5-carboxylate Reductase, and have been seen in publications frequently: Cognition, Excretion, Proline Transport, Synaptic Transmission, Transport

Quite a number of genes have been found to play important roles in Deficiency Of Pyrroline-5-carboxylate Reductase, such as ACHE, ALDH4A1, CA1, CA3, CAT, CD40LG, CSF2, DLC1, GLYAT, LAMC2, NDUFAB1, PDXP, PLP1, PNPO, PRDX5, SCYL1, SOD1, TDRD7, TRAF2. See what Boster has to offer for the research of these genes by clicking the gene name links below and view a more detailed info card/product listing for that gene.

In a later update, we will include information such as current drugs and therapy solutions as well as on-going and past clinical trials for this disease. Plesae stay updated.

Deficiency Of Pyrroline-5-carboxylate Reductase Related Genes

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Pathways Related to Deficiency Of Pyrroline-5-carboxylate Reductase

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