Human Genome Epidemiology Literature Finder
Rare Diseases
Records 1 - 4 (of 4 Records) |
Query Trace: Urea Cycle Disorders[original query] |
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Genotype-Phenotype Correlations in Ornithine Transcarbamylase Deficiency: A Mutation Update. Journal of genetics and genomics = Yi chuan xue bao 2015 May 42 (5): 181-94. Caldovic Ljubica, Abdikarim Iman, Narain Sahas, Tuchman Mendel, Morizono Hiro |
Low prevalence of argininosuccinate lyase deficiency among inherited urea cycle disorders in Korea. Journal of human genetics 2018 5 63 (8): 911-917. Kim Dahye, Ko Jung Min, Kim Yoon-Myung, Seo Go Hun, Kim Gu-Hwan, Lee Beom Hee, Yoo Han-Wo |
Urea cycle disorders in Argentine patients: clinical presentation, biochemical and genetic findings. Orphanet journal of rare diseases 2019 Aug 14 (1): 203. Silvera-Ruiz Silene M, Arranz José A, Häberle Johannes, Angaroni Celia J, Bezard Miriam, Guelbert Norberto, Becerra Adriana, Peralta Fernanda, de Kremer Raquel Dodelson, Laróvere Laura |
Retrospective evaluation of 85 patients with urea cycle disorders: one center experience, three new mutations. Journal of pediatric endocrinology & metabolism : JPEM 2020 5 33 (6): 721-728. Sarita? Nakip Özlem, Y?ld?z Y?lmaz, Tokatl? Ay?eg |
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- Page last updated:May 13, 2024
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