Journal article Published 2016
Significant phenotype variability of congenital central hypoventilation syndrome in a family with polyalanine expansion mutation of the PHOX2B gene
Biomedical Papers of the Medical Faculty of the University Palacký, Olomouc, Czech Republic 160(4), 495-498 (2016)
- 2016 Year
- 27485184 PMID
Cite this publication
KLASKOVA, E., J. DRÁBEK, M. HOBZOVA, V. SMOLKA, M. SEDA, J. HYJÁNEK, R. SLAVKOVSKÝ, J. STRÁNSKÁ, M. PROCHAZKA: Significant phenotype variability of congenital central hypoventilation syndrome in a family with polyalanine expansion mutation of the PHOX2B gene. Biomedical Papers of the Medical Faculty of the University Palacký, Olomouc, Czech Republic. 2016, 160(4), 495-498, ISSN: 1213-8118, PMID: 27485184.
Details
- ISSN
- 1213-8118
