Rare α(0)-thalassemia deletions detected by MLPA in five unrelated Brazilian patients

Alpha-thalassemias are among the most common genetic diseases in the world. They are characterized by hypochromic and microcytic anemia and great clinical variability, ranging from a practically asymptomatic phenotype to severe anemia, which can lead to intrauterine or early neonatal death. Deletion...

Πλήρης περιγραφή

Αποθηκεύτηκε σε:
Λεπτομέρειες βιβλιογραφικής εγγραφής
Τόπος έκδοσης:Genet Mol Biol
Κύριοι συγγραφείς: Mota, Natália O., Kimura, Elza M., Ferreira, Roberta D., Pedroso, Gisele A., Albuquerque, Dulcinéia M., Ribeiro, Daniela M., Santos, Magnun N. N., Bittar, Cristina M., Costa, Fernando F., Sonati, Maria de Fatima
Μορφή: Artigo
Γλώσσα:Inglês
Έκδοση: Sociedade Brasileira de Genética 2017
Θέματα:
Human and Medical Genetics
Διαθέσιμο Online:https://ncbi.nlm.nih.gov/pmc/articles/PMC5738609/
https://ncbi.nlm.nih.gov/pubmed/28981562
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1590/1678-4685-GMB-2016-0330
Ετικέτες: Προσθήκη ετικέτας
Δεν υπάρχουν, Καταχωρήστε ετικέτα πρώτοι!

Παρόμοια τεκμήρια