Severe hereditary haemolytic anaemia in a Caucasian newborn: a new fetal haemoglobin variant Hb F-Bonheiden ((G)gamma 38(C4) Thr-->Pro).

Article Details

Citation

Van den Driessche M, Moerman J, Moens M, Van Eldere S, Derclaye I, Philippe M

Severe hereditary haemolytic anaemia in a Caucasian newborn: a new fetal haemoglobin variant Hb F-Bonheiden ((G)gamma 38(C4) Thr-->Pro).

Eur J Pediatr. 2005 Apr;164(4):261-2. Epub 2005 Jan 12.

PubMed ID
15645283 [ View in PubMed
]
Abstract

Not Available

DrugBank Data that Cites this Article

Polypeptides
NameUniProt ID
Hemoglobin subunit gamma-2P69892Details