(Q24600356)

English

Carbonic anhydrase II deficiency identified as the primary defect in the autosomal recessive syndrome of osteopetrosis with renal tubular acidosis and cerebral calcification

scientific article

Statements

Carbonic anhydrase II deficiency identified as the primary defect in the autosomal recessive syndrome of osteopetrosis with renal tubular acidosis and cerebral calcification (English)
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W S Sly
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D Hewett-Emmett
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M P Whyte
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Y S Yu
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R E Tashian
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May 1983
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80
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2752-6
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9
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Identifiers

 
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