arginine and Familial Hypobetalipoproteinemia

arginine has been researched along with Familial Hypobetalipoproteinemia in 1 studies

Research

Studies (1)

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

Authors

Authors	Studies
Burnett, JR; Hegele, RA; McKnight, CJ; Miskie, BA; Shan, J; Tran, K; Whitfield, AJ; Yao, Z; Yuan, J	1

Other Studies

1 other study(ies) available for arginine and Familial Hypobetalipoproteinemia

Article	Year
A novel nontruncating APOB gene mutation, R463W, causes familial hypobetalipoproteinemia. The Journal of biological chemistry, 2003, Apr-11, Volume: 278, Issue:15 Topics: Amino Acid Substitution; Apolipoprotein B-100; Apolipoprotein B-48; Apolipoproteins B; Arginine; Base Sequence; Female; Genetic Carrier Screening; Humans; Hypobetalipoproteinemias; Male; Models, Molecular; Mutation, Missense; Oligodeoxyribonucleotides; Pedigree; Point Mutation; Protein Conformation	2003

Article

Year

A novel nontruncating APOB gene mutation, R463W, causes familial hypobetalipoproteinemia.

The Journal of biological chemistry, 2003, Apr-11, Volume: 278, Issue:15

Topics: Amino Acid Substitution; Apolipoprotein B-100; Apolipoprotein B-48; Apolipoproteins B; Arginine; Base Sequence; Female; Genetic Carrier Screening; Humans; Hypobetalipoproteinemias; Male; Models, Molecular; Mutation, Missense; Oligodeoxyribonucleotides; Pedigree; Point Mutation; Protein Conformation

2003