Carbonic anhydrase II deficiency identified as the primary defect in the autosomal recessive syndrome of osteopetrosis with renal tubular acidosis and cerebral calcification
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| Description | scientific article |
| Author/s |
author: Michael P. Whyte |
| Publication date | May 1983 |
| Language | English |
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| Wikipedia link | |
| Copyright status | |
| Missing/wrong data? | Edit Wikidata item |