| Literature DB >> 17994382 |
Kamran Moradkhani1, Joan Henthorn, Jean Riou, Lorraine Phelan, Claude Préhu, Henri Wajcman.
Abstract
We present a new case of Hb Niigata that we named Hb Niigata(C), observed in a woman from Romania, with a mutation different from that described in Japanese (GTG-->CTG instead of GTG-->TTG). This single nucleotide substitution replaces the valine residue for leucine at codon 1 and causes retention of the N-terminal methionine leading to an elongated beta chain. This mutation was without any hematological consequences.Entities:
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Year: 2007 PMID: 17994382 DOI: 10.1080/03630260701587885
Source DB: PubMed Journal: Hemoglobin ISSN: 0363-0269 Impact factor: 0.849