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COQ6 mutations in patients with nephrotic syndrom, sensorineural deafness and optical atrophy

Document Type

Journal

Author

Rousset-Rouviere, Caroline; Boyer, Olivia; Caillez, Mathilde; Garaix, Florentine; Cano, A.; Gribouval, Olivier; Antignac, Corinne; Tsimaratos, Michel

Source

PEDIATRIC NEPHROLOGY; AUG 2013, 28 8, p1458-p1458, 1p.

Subject

Language

English

ISSN

1432198X

Online Access

Full Text (Springer-Archive) Full Text (Gale Academic Onefile) Full Text (Gale General Onefile) Web of Science JCR 저널정보 Scopus Find it@PNU

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