Φορτώνει......

Harderoporphyria: Case of lifelong photosensitivity associated with compound heterozygous coproporphyrinogen oxidase (CPOX) mutations

A 78-year-old man with a history of neonatal anemia and jaundice and life-long photosensitivity was found to have harderoporphyria, as evidenced by increased porphyrins in urine, plasma, erythrocytes and feces including large amounts of harderoporphyrin in feces and erythrocytes. Two previously unde...

Πλήρης περιγραφή

Αποθηκεύτηκε σε:
Λεπτομέρειες βιβλιογραφικής εγγραφής
Κύριοι συγγραφείς: A. Moghe, V.M.S. Ramanujam, J.D. Phillips, R.J. Desnick, K.E. Anderson
Μορφή: Artigo
Γλώσσα:Inglês
Έκδοση: Elsevier 2019-06-01
Σειρά:Molecular Genetics and Metabolism Reports
Διαθέσιμο Online:http://www.sciencedirect.com/science/article/pii/S2214426918301484
Ετικέτες: Προσθήκη ετικέτας
Δεν υπάρχουν, Καταχωρήστε ετικέτα πρώτοι!