Compound effect of PHOX2B and RET gene variants in congenital central hypoventilation syndrome combined with hirschsprung disease
Research output: Contribution to journal › Letter › Contributed › peer-review
Details
Original language | English |
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Pages (from-to) | 1486-1489 |
Number of pages | 4 |
Journal | American Journal of Medical Genetics, Part A |
Volume | 146 |
Issue number | 11 |
Publication status | Published - 1 Jun 2008 |
Peer-reviewed | Yes |
External IDs
PubMed | 18438890 |
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