TY  - GEN
AU  - Daga,Ankana
AU  - Majmundar,Amar J
AU  - Braun,Daniela A
AU  - Gee,Heon Yung
AU  - Lawson,Jennifer A
AU  - Shril,Shirlee
AU  - Jobst-Schwan,Tilman
AU  - Vivante,Asaf
AU  - Schapiro,David
AU  - Tan,Weizhen
AU  - Warejko,Jillian K
AU  - Widmeier,Eugen
AU  - Nelson,Caleb P
AU  - Fathy,Hanan M
AU  - Gucev,Zoran
AU  - Soliman,Neveen A
AU  - Hashmi,Seema
AU  - Halbritter,Jan
AU  - Halty,Margarita
AU  - Kari,Jameela A
AU  - El-Desoky,Sherif
AU  - Ferguson,Michael A
AU  - Somers,Michael J G
AU  - Traum,Avram Z
AU  - Stein,Deborah R
AU  - Daouk,Ghaleb H
AU  - Rodig,Nancy M
AU  - Katz,Avi
AU  - Hanna,Christian
AU  - Schwaderer,Andrew L
AU  - Sayer,John A
AU  - Wassner,Ari J
AU  - Mane,Shrikant
AU  - Lifton,Richard P
AU  - Milosevic,Danko
AU  - Tasic,Velibor
AU  - Baum,Michelle A
AU  - Hildebrandt,Friedhelm
TI  - Whole exome sequencing frequently detects a monogenic cause in early onset nephrolithiasis and nephrocalcinosis
SN  - 1523-1755
PY  - 2018///1211
KW  - Adolescent
KW  - Age of Onset
KW  - Child
KW  - Child, Preschool
KW  - Disease Progression
KW  - Female
KW  - Genetic Association Studies
KW  - Genetic Markers
KW  - Genetic Predisposition to Disease
KW  - Heredity
KW  - Humans
KW  - Infant
KW  - Male
KW  - Mutation
KW  - Nephrocalcinosis
KW  - diagnostic imaging
KW  - Nephrolithiasis
KW  - Pedigree
KW  - Phenotype
KW  - Predictive Value of Tests
KW  - Prognosis
KW  - Risk Factors
KW  - Tomography, X-Ray Computed
KW  - Ultrasonography
KW  - Exome Sequencing
KW  - Young Adult
N1  - Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1016/j.kint.2017.06.025
ER  -