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Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1961 1
1964 1
1967 2
1970 1
1973 1
1976 2
1978 3
1979 1
1980 1
1981 1
1984 1
1986 2
1988 2
1989 1
1990 2
1991 3
1992 1
2002 2
2023 0

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PubMed (OMIM) for id: 78687

28 results

Results by year

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Page 1
Clinical, enzymatic, and molecular genetic characterization of a biochemical variant type of argininosuccinic aciduria: prenatal and postnatal diagnosis in five unrelated families.
Kleijer WJ, Garritsen VH, Linnebank M, Mooyer P, Huijmans JG, Mustonen A, Simola KO, Arslan-Kirchner M, Battini R, Briones P, Cardo E, Mandel H, Tschiedel E, Wanders RJ, Koch HG. Kleijer WJ, et al. J Inherit Metab Dis. 2002 Sep;25(5):399-410. doi: 10.1023/a:1020108002877. J Inherit Metab Dis. 2002. PMID: 12408190
Arginosuccine aciduria.
Levin B. Levin B. Am J Dis Child. 1967 Jan;113(1):162-5. Am J Dis Child. 1967. PMID: 6015896 No abstract available.
A familial study of a human enzyme defect, argininosuccinic aciduria.
Coryell ME, Hall WK, Thevaos TG, Welter DA, Gatz AJ, Horton BF, Sisson BD, Looper JW Jr, Farrow RT. Coryell ME, et al. Biochem Biophys Res Commun. 1964;14:307-12. doi: 10.1016/s0006-291x(64)80001-2. Biochem Biophys Res Commun. 1964. PMID: 5836520 No abstract available.
28 results