Relevance of SOX17 variants for hypomyelinating leukodystrophies and congenital anomalies of the kidney and urinary tract (CAKUT).

Combes, Patricia

Relevance of SOX17 variants for hypomyelinating leukodystrophies and congenital anomalies of the kidney and urinary tract (CAKUT). [electronic resource] - Annals of human genetics May 2012 - 261-7 p. digital

Publication Type: Journal Article; Research Support, Non-U.S. Gov't

1469-1809

10.1111/j.1469-1809.2011.00702.x doi


Child
Child, Preschool
Female
Genetic Variation
Hereditary Central Nervous System Demyelinating Diseases--genetics
Humans
Kidney--abnormalities
Male
SOXF Transcription Factors--genetics
Urinary Tract--abnormalities