tryptophan and Elliptocytosis, Hereditary

tryptophan has been researched along with Elliptocytosis, Hereditary in 1 studies

Research

Studies (1)

Timeframe	Studies, this research(%)	All Research%
pre-1990	1 (100.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Delaunay, J; Denoroy, L; Dhermy, D; Forget, BG; Garbarz, M; Godet, J; Kastally, R; Morlé, F; Morlé, L; Roux, AF	1

Other Studies

1 other study(ies) available for tryptophan and Elliptocytosis, Hereditary

Article	Year
Spectrin Tunis (Sp alpha I/78), an elliptocytogenic variant, is due to the CGG----TGG codon change (Arg----Trp) at position 35 of the alpha I domain. Blood, 1989, Aug-01, Volume: 74, Issue:2 Topics: Amino Acid Sequence; Arginine; Base Sequence; Codon; Elliptocytosis, Hereditary; Gene Amplification; Genetic Variation; Haplotypes; Molecular Sequence Data; Mutation; Peptide Fragments; Polymorphism, Restriction Fragment Length; RNA, Messenger; Spectrin; Tryptophan	1989

Article

Year

Spectrin Tunis (Sp alpha I/78), an elliptocytogenic variant, is due to the CGG----TGG codon change (Arg----Trp) at position 35 of the alpha I domain.

Blood, 1989, Aug-01, Volume: 74, Issue:2

Topics: Amino Acid Sequence; Arginine; Base Sequence; Codon; Elliptocytosis, Hereditary; Gene Amplification; Genetic Variation; Haplotypes; Molecular Sequence Data; Mutation; Peptide Fragments; Polymorphism, Restriction Fragment Length; RNA, Messenger; Spectrin; Tryptophan

1989