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Paper Details

A Frame-Shift Mutation in CAV1 Is Associated with a Severe Neonatal Progeroid and Lipodystrophy Syndrome.
PLoS One
31
2015
Author NameAffiliation
Szabolcs SzelingerCenter for Rare Childhood Disorders, Translational Genomics Research Institute
Ivana MalenicaCenter for Rare Childhood Disorders, Translational Genomics Research Institute
David W CraigCenter for Rare Childhood Disorders, Translational Genomics Research Institute
Matthew J HuentelmanCenter for Rare Childhood Disorders, Translational Genomics Research Institute
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Release 1.2