Article info
Genotype-phenotype correlations
Original article
Hemizygous mutations in SNAP29 unmask autosomal recessive conditions and contribute to atypical findings in patients with 22q11.2DS
- Correspondence to Dr Loydie A Jerome-Majewska, Department of Pediatrics and Human Genetics, McGill University Research Institute, Place Toulon, 4060 Ste Catherine West PT 420, Montreal, QC H3Z 2Z3, Canada; loydie.majewska{at}mcgill.ca
Citation
Hemizygous mutations in SNAP29 unmask autosomal recessive conditions and contribute to atypical findings in patients with 22q11.2DS
Publication history
- Received September 24, 2012
- Revised November 10, 2012
- Accepted November 13, 2012
- First published December 11, 2012.
Online issue publication
January 20, 2013
Article Versions
- Previous version (11 December 2012).
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Files in this Data Supplement:
- Data supplement 1 - Online supplement
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