Aspartylglycosaminuri or aspartylglucosaminuria Treff i utvalgte kilder: [Skjul boksen]
  1. bmj-bestpractice
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    https://bestpractice.bmj.com/topics/en-gb/1021/aetiology
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    ... type 2 (acid maltase deficiency). Glycoproteinoses (e.g., aspartylglucosaminuria, fucosidosis, alpha- and beta-mannosidosis, Schindler's disease) ... UK: Adis International Communications; 2004. Glycoproteinoses (e.g., aspartylglucosaminuria, fucosidosis, alpha- and beta-mannosidosis, Schindler's disease) ...
  2. bmj-bestpractice
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    https://bestpractice.bmj.com/topics/en-gb/1021/pdf/1021.pdf
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    ... type 2 (acid maltase deficiency). • Glycoproteinoses (e.g., aspartylglucosaminuria, fucosidosis, alpha- and beta-mannosidosis, Schindler's disease) • ... 100,000 people[ 5] [ 6] • Glycoproteinoses (e.g., aspartylglucosaminuria, fucosidosis, alpha- and beta-mannosidosis, Schindler's disease) • ...
  3. bmj-bestpractice
    -
    https://bestpractice.bmj.com/topics/en-us/1021/pdf/1021.pdf
    /
    ... type II (acid maltase deficiency). • Glycoproteinoses (e.g., aspartylglucosaminuria, fucosidosis, alpha and beta mannosidosis, Schindler disease) • Multiple ...