Carbonic anhydrase II deficiency in 12 families with the autosomal recessive syndrome of osteopetrosis with renal tubular acidosis and cerebral calcification.
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D. Hewett‐Emmett | W. Sly | M. Whyte | V. Sundaram | R. Tashian | A. Ohlsson | M. Al-Mosawi | A. Gruskin | P. Guibaud | H. Baluarte | N. Sakati | M. Vainsel