Author:
Ichisaka Satoshi,Ohno Kousaku,Yuasa Isao,Nanba Eiji,Sakuraba Hitoshi,Suzuki Yoshiyuki
Subject
Neurology (clinical),Developmental Neuroscience,General Medicine,Pediatrics, Perinatology and Child Health
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5. Mutation in PMM2, a phosphomannomutase gene on chromosome 16p13, in carbohydrate-deficient glycoprotein type I syndrome (Jaeken syndrome);Matthis;Nat Genet,1997
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