arginine and Congenital Hypocupremia

arginine has been researched along with Congenital Hypocupremia 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	0 (0.00)	29.6817
2010's	1 (100.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Endreffy, E; Horn, N; László, A; Szabó, J; Tümer, Z	1

Other Studies

1 other study(ies) available for arginine and Congenital Hypocupremia

Article	Year
Molecular genetic mutation analysis in Menkes-disease with prenatal diagnosis. Ideggyogyaszati szemle, 2010, Jan-30, Volume: 63, Issue:1-2 Topics: Adenosine Triphosphatases; Arginine; Cation Transport Proteins; Chorionic Villi Sampling; Copper-Transporting ATPases; DNA Mutational Analysis; Exons; Fatal Outcome; Female; Heterozygote; Histidine; Humans; Infant; Male; Menkes Kinky Hair Syndrome; Mutation, Missense; Polymerase Chain Reaction; Prenatal Diagnosis; Young Adult	2010

Article

Year

Molecular genetic mutation analysis in Menkes-disease with prenatal diagnosis.

Ideggyogyaszati szemle, 2010, Jan-30, Volume: 63, Issue:1-2

Topics: Adenosine Triphosphatases; Arginine; Cation Transport Proteins; Chorionic Villi Sampling; Copper-Transporting ATPases; DNA Mutational Analysis; Exons; Fatal Outcome; Female; Heterozygote; Histidine; Humans; Infant; Male; Menkes Kinky Hair Syndrome; Mutation, Missense; Polymerase Chain Reaction; Prenatal Diagnosis; Young Adult

2010