Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney Malformations.

Sanna-Cherchi, Simone

Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney Malformations. [electronic resource] - American journal of human genetics Nov 2017 - 789-802 p. digital

Publication Type: Journal Article

1537-6605

10.1016/j.ajhg.2017.09.018 doi


Alleles
Animals
Case-Control Studies
Clustered Regularly Interspaced Short Palindromic Repeats--genetics
Congenital Abnormalities--genetics
Exome--genetics
Female
Genetic Heterogeneity
Genome-Wide Association Study--methods
Genotype
Heredity--genetics
Homozygote
Humans
Kidney--abnormalities
Kidney Diseases--congenital
Male
Membrane Proteins--genetics
Mice
Mutation--genetics
Neoplasm Proteins--genetics
Phenotype
RNA, Long Noncoding--genetics
Urinary Tract--abnormalities
Urogenital Abnormalities--genetics
Zebrafish