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  1. 1
    Clinical features and follow-up study on 55 patients with adolescence-onset methylmalonic acidemia

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  2. 2
    Analysis of the regional distribution differences of common variations of the MMACHC gene in cblC methylmalonic acidemia patients

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  3. 3
    Clinical and genetic studies on 76 patients with hydrocephalus caused by methylmalonic acidemia combined with homocysteinuria

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  4. 4
    Screening for carriers of pathogenic genes for methylmalonic acidemia and Wilson's disease in neonates in Qingdao

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  5. 5
    Clinical analysis of methylmalonic acidemia and hyperhomocysteinemia with diffuse lung disease as an initial or main presentation

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  6. 6
    Heterogeneous phenotypes, genotypes, treatment and prevention of 1 003 patients with methylmalonic acidemia in the mainland of China

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  7. 7
    Advances in the clinical and laboratory studies on methylmalonic aciduria combined with homocysteinemia type cblC
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  8. 8
    Analysis of clinical features and gene mutations in two Chinese pedigrees with late-onset methylmalonic acidemia, cblC type
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