Hereditary non-spherocytic haemolytic anaemia with post-splenectomy inclusion bodies and pigmenturia caused by an unstable haemoglobin Santa Ana-beta-88 (F4) leucine--proline.

Author:

Opfell R W,Lorkin P A,Lehmann H

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference18 articles.

1. A partial amino sequence for sheep haemoglobin A;Beale, D.;Biochem. 7,1967

2. Haemoglobin M Hyde Park; a hereditary methaemoglobinaemia in a Caucasian;Becroft, D.M.O.; Douglas, R.; Carrell, R.W.; Lehmann, H.;N. Z. med. J7,1968

3. Hemoglobin Gun Hill: deletion of five amino acid residues and impaired heme-globin binding;Bradley, T.B.; Wohl, R.C.; Rieder, R.F.;Science,1967

4. Haemoglobin Koln (1-98 valine-smethionine): an unstable protein causing inclusion body anaemia;Carrell, R.W.; Lehmann, H.; Hutchison, H.E.;Nature (Lond.); Haemoglobin,1966

5. Abnormal human haemoglobins. Separation and characterization of the a and chains by chromatography, and the determination of two new variants, Hb;Clegg, J.B.; Naughton, M.A.; Weatherall, D.J.;Chesapeake and Hb J (Bangkok). J. molec. Biol,1966

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