IV-a.   Nondeletional Hereditary Persistence of Fetal Hemoglobin (HPFH)

-202 (C->G) Ggamma; nd-HPFH
-202 (C->T) Agamma; nd-HPFH
-200 (+C) Ggamma; the Tunisian nd-HPFH
-198 (T->C) Agamma; the British nd-HPFH
-196 (C->T) Agamma; the Italian nd-HPFH
-195 (C->G) Agamma; the Brazilian nd-HPFH
-175 (T->C) Ggamma; nd-HPFH
-175 (T->C) Agamma; the Black nd-HPFH
-117 (G->A) Agamma; the Greek-Italian nd-HPFH
-117 (G->A) Agamma; the Black-Greek nd-HPFH
-114 (C->G) Ggamma; the Australian nd-HPFH
-114 (C->T) Ggamma; the Japanese nd-HPFH
-114 (C->T) Agamma; the Georgia nd-HPFH
-110 (A->C) Ggamma; the Czech nd-HPFH
The 13 bp deletion (-CAATAGCCTTGAC at -114 through -102)

This material is from the book A Syllabus of Thalassemia Mutations (1997) by Titus H.J. Huisman, Marianne F.H. Carver, and Erol Baysal, published by The Sickle Cell Anemia Foundation in Augusta, GA, USA. Copyright © 1997 by Titus H.J. Huisman. All rights reserved. Neither this work nor any part may be reproduced or transmitted in any form or by any means, electronic or mechanical, microfilming and recording, or by any information storage and retrieval systems, without permission in writing from the Author.