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New type ékho-12 portable echoencephalograph

✍ Scribed by N. K. Bogolepov; V. E. Grechko; V. A. Ter-Simonyan; N. M. Florianovich; I. A. Skorunskii; A. M. Tauluev

Book ID
104810530
Publisher
Springer US
Year
1973
Tongue
English
Weight
336 KB
Volume
7
Category
Article
ISSN
0006-3398

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Mucopolysaccharidosis III D (Sanfilippo disease type D, MPS IIID) is a rare autosomal recessive lysosomal storage disorder previously described in only 20 patients. MPS IIID is caused by a deficiency of N-acetylglucosamine-6-sulphate sulphatase (GNS), one of the enzymes required for the degradation