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7. [Studies of a case of aminoacidopathy due to isolated hypervalinemia]. Burdea M; Tănase-Mogoş I; Rusu I; Cirdei E; Gaiginschi N Physiologie; 1979; 16(2):123-8. PubMed ID: 117465 [No Abstract] [Full Text] [Related]
8. Lysinuric protein intolerance, an autosomal recessive disease. A genetic study of 10 Finnish families. Norio R; Perheentupa J; Kekomäki M; Visakorpi JK Clin Genet; 1971; 2(4):214-22. PubMed ID: 5146580 [No Abstract] [Full Text] [Related]
10. Type II hyperprolinaemia in a pedigree of Irish travellers (nomads). Flynn MP; Martin MC; Moore PT; Stafford JA; Fleming GA; Phang JM Arch Dis Child; 1989 Dec; 64(12):1699-707. PubMed ID: 2624476 [TBL] [Abstract][Full Text] [Related]
11. Hyperprolinaemia in two successive generations of a North American Indian family. Perry TL; Hardwick DF; Lowry RB; Hansen S Ann Hum Genet; 1968 May; 31(4):401-7. PubMed ID: 4299764 [No Abstract] [Full Text] [Related]