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Whole Exome Sequencing in Patients with the Cuticular Drusen Subtype of Age-Related Macular DegenerationPhenotype Characteristics of Patients With Age-Related Macular Degeneration Carrying a Rare Variant in the Complement Factor H Gene.The complement system in age-related macular degeneration: A review of rare genetic variants and implications for personalized treatment.The Functional Effect of Rare Variants in Complement Genes on C3b Degradation in Patients With Age-Related Macular Degeneration.Rare Genetic Variants Associated With Development of Age-Related Macular Degeneration.Genome-Wide Association Study Reveals Variants in CFH and CFHR4 Associated with Systemic Complement Activation: Implications in Age-Related Macular Degeneration.Monocarboxylate transporter 1 deficiency and ketone utilizationFunctional analyses of rare genetic variants in complement component C9 identified in patients with age-related macular degenerationGenetic screening for macular dystrophies in patients clinically diagnosed with dry age-related macular degenerationGenotype-phenotype correlations of low-frequency variants in the complement system in renal disease and age-related macular degenerationMacular Dystrophy and Cone-Rod Dystrophy Caused by Mutations in the RP1 Gene: Extending the RP1 Disease SpectrumAn FDA-Approved Drug Screen for Compounds Influencing Craniofacial Skeletal Development and Craniosynostosis
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P50
description
hulumtuese
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Maartje J Geerlings
@ast
Maartje J Geerlings
@en
Maartje J Geerlings
@es
Maartje J Geerlings
@nl
Maartje J Geerlings
@sl
type
label
Maartje J Geerlings
@ast
Maartje J Geerlings
@en
Maartje J Geerlings
@es
Maartje J Geerlings
@nl
Maartje J Geerlings
@sl
prefLabel
Maartje J Geerlings
@ast
Maartje J Geerlings
@en
Maartje J Geerlings
@es
Maartje J Geerlings
@nl
Maartje J Geerlings
@sl
P1053
P-8309-2015
P106
P21
P31
P3829
P496
0000-0003-1164-3573
P569
2000-01-01T00:00:00Z