cysteine and Asplenia Syndrome

cysteine has been researched along with Asplenia Syndrome 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
Akdemir, ZC; Azamian, MS; Belmont, JW; Braxton, A; Chandarana, J; D'Alessandro, LC; Ding, Y; Eldomery, MK; Eng, CM; Gibbs, RA; Hanchard, NA; Harel, T; Holtzman, J; Jhangiani, SN; Kois, C; Lupski, JR; Miller, K; Muzny, DM; Rijhsinghani, A; Rosenfeld, JA; Sack, V; Shur, N; Vetrini, F; Yang, Y	1

Other Studies

1 other study(ies) available for cysteine and Asplenia Syndrome

Article	Year
Bi-allelic Mutations in PKD1L1 Are Associated with Laterality Defects in Humans. American journal of human genetics, 2016, Oct-06, Volume: 99, Issue:4 Topics: Alleles; Amino Acid Motifs; Amino Acid Sequence; Animals; Caenorhabditis elegans; Cysteine; Exome; Female; Fetal Diseases; Functional Laterality; Heart Defects, Congenital; Heterotaxy Syndrome; Homozygote; Humans; Infant, Newborn; Introns; Male; Membrane Proteins; Mice; Middle Aged; Models, Molecular; Mutation; Mutation, Missense; Oryzias; Pedigree; RNA Splicing; Situs Inversus	2016

Article

Year

Bi-allelic Mutations in PKD1L1 Are Associated with Laterality Defects in Humans.

American journal of human genetics, 2016, Oct-06, Volume: 99, Issue:4

Topics: Alleles; Amino Acid Motifs; Amino Acid Sequence; Animals; Caenorhabditis elegans; Cysteine; Exome; Female; Fetal Diseases; Functional Laterality; Heart Defects, Congenital; Heterotaxy Syndrome; Homozygote; Humans; Infant, Newborn; Introns; Male; Membrane Proteins; Mice; Middle Aged; Models, Molecular; Mutation; Mutation, Missense; Oryzias; Pedigree; RNA Splicing; Situs Inversus

2016