A PEX6-Defective Peroxisomal Biogenesis Disorder with Severe Phenotype in an Infant, versus Mild Phenotype Resembling Usher Syndrome in the Affected Parents
- 1 April 2002
- journal article
- case report
- Published by Elsevier BV in American Journal of Human Genetics
- Vol. 70 (4), 1062-1068
- https://doi.org/10.1086/339766
Abstract
No abstract availableKeywords
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