Whole exome sequencing reveals two novel mutations in GREB1L in two Chinese families with renal agenesis.

Subjects

Subjects :

Female
Humans
Male
China
Congenital Abnormalities
East Asian People
Kidney abnormalities
Kidney diagnostic imaging
Kidney Diseases congenital
Neoplasm Proteins
Asian People genetics
Exome Sequencing
Mutation
Pedigree

Details

Language :

English

ISSN :

1460-2393

Volume :

117

Issue :

6

Database :

MEDLINE

Journal :

QJM : monthly journal of the Association of Physicians

Publication Type :

Academic Journal

Accession number :

38410081

Full Text :

https://doi.org/10.1093/qjmed/hcae036