TY  - GEN
AU  - Combes,Patricia
AU  - Planche,Vincent
AU  - Eymard-Pierre,Eléonore
AU  - Sarret,Catherine
AU  - Rodriguez,Diana
AU  - Boespflug-Tanguy,Odile
AU  - Vaurs-Barriere,Catherine
TI  - Relevance of SOX17 variants for hypomyelinating leukodystrophies and congenital anomalies of the kidney and urinary tract (CAKUT)
SN  - 1469-1809
PY  - 2012///0629
KW  - Child
KW  - Child, Preschool
KW  - Female
KW  - Genetic Variation
KW  - Hereditary Central Nervous System Demyelinating Diseases
KW  - genetics
KW  - Humans
KW  - Kidney
KW  - abnormalities
KW  - Male
KW  - SOXF Transcription Factors
KW  - Urinary Tract
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1111/j.1469-1809.2011.00702.x
ER  -