Chemical Modification of Carbonic Anhydrase II with Acrolein
نویسندگان
چکیده
منابع مشابه
Carbonic anhydrase II deficiency a novel mutation.
Carbonic anhydrase II (CA II) deficiency is an extremely rare autosomal recessive disorder, characterised by a triad of osteopetrosis, renal tubular acidosis and cerebral calcifications. A 12 year old boy with classical features of CA II deficiency is reported who was found to be homozygous for the mutation in CA II gene and parents were heterozygous for the same mutation .To the best of our kn...
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متن کاملOrganization of the mouse and human carbonic anhydrase II genes.
The carbonic anhydrase (CA) multigene family is beginning to appear more complex than was considered possible during the earlier days of work on the different isozymes. The two classic erythrocyte isozymes found in amniotes, CA I and CA 11, have been studied in considerable detail in terms of their kinetics, structures, and Within the last few years, at least one other isozyme (CA 111), which i...
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ژورنال
عنوان ژورنال: Journal of Biological Chemistry
سال: 1989
ISSN: 0021-9258
DOI: 10.1016/s0021-9258(18)63871-2