Carbonic anhydrase II deficiency syndrome in a Belgian family is caused by a point mutation at an invariant histidine residue (107 His----Tyr): complete structure of the normal human CA II gene (Q24678433)
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(P31) (Q13442814)
(P304) 1082-90
(P407) (Q1860)
(P433) 5
(P478) 49
(P577) +1991-11-00T00:00:00Z
(P1433) (Q4744249)
(P1476) "Carbonic anhydrase II deficiency syndrome in a Belgian family is caused by a point mutation at an invariant histidine residue (107 His----Tyr): complete structure of the normal human CA II gene" (language: en)
(P2093) P J Venta
R J Welty
T M Johnson
W S Sly
R E Tashian
(P2860) (Q24600356)
(Q24626779)
(Q24557511)
(Q24564676)
(Q24561689)
(Q27860696)
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(Q28307228)
(Q28290804)
(Q28290513)
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(Q28281740)
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(Q29620173)
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(Q29620525)
(Q36873069)
(Q33560944)
(Q36426444)
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