grenade 发表于 2025-3-23 09:46:19

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简略 发表于 2025-3-23 14:43:09

Storia di Roberta e dei Suoi Giochi,n storage disease type III improve. However, there was a high incidence of myopathy and cardiomyopathy. Patients with glycogen storage disease types VI and IX had a normal growth pattern after childhood. Hepatomegaly and hypercholesterolaemia, however, were still present in half of the patients.

RACE 发表于 2025-3-23 21:53:30

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Prologue 发表于 2025-3-23 22:47:52

,La Fatina Spargiluce e L’orco Mezzanotte, gene. The . subunit gene was mapped to chromosome Xq12-q13 and the . subunit gene to chromosome 16q12-q13. Isoform cDNAs reveal differential mRNA splicing. Thus, the stage is set for the molecular characterization of the genes and their deficiency mutations.

GEM 发表于 2025-3-24 05:10:44

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先行 发表于 2025-3-24 10:34:43

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RAG 发表于 2025-3-24 10:59:50

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OATH 发表于 2025-3-24 17:19:52

Book 1990also attended on "Maternal Phenylketonuria", organized by Dr the highly interesting workshop D. Brenton, London. This four-hour workshop included international practical experiences in the treatment of maternal phenylketonuria as well as the results of amino acid transport and animal experiments.

使无效 发表于 2025-3-24 23:05:21

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RECUR 发表于 2025-3-25 02:10:20

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查看完整版本: Titlebook: Carbohydrate and Glycoprotein Metabolism; Maternal Phenylketonuria; R. A. Harkness,R. J. Pollitt,G. M. Addison Book 1990 Society for the S