Genetic studies

CM Cinta Moraleda
RA Ruth Aguilar
LQ Llorenç Quintó
TN Tacilta Nhampossa
MR Montserrat Renom
AN Augusto Nhabomba
SA Sozinho Acácio
JA John J. Aponte
DN Delino Nhalungo
AA Ariel H. Achtman
LS Louis Schofield
HM Helder Martins
EM Eusebio Macete
PA Pedro L. Alonso
CM Clara Menéndez
ask Ask a question
Favorite

Haemoglobinopathies and β-thalassaemia were assessed using the β-thalassaemia Short Program from the Variant Haemoglobin Testing System® (Bio-Rad, Hercules, USA). Detection of α-thalassaemia (3.7 kb deletion) was performed by the GAP-PCR method [20]. Glucose 6-phosphate dehydrogenase (G6PD) deficiency was determined using the Beutler fluorescent spot test [21].

Do you have any questions about this protocol?

Post your question to gather feedback from the community. We will also invite the authors of this article to respond.

post Post a Question
0 Q&A