Remarkable Genetic Finding in a Girl with Phenotype of Classic Pelizäus-Merzbacher Disease: Xq22.2 Microdeletion Including PLP1 and Other Genes
Christiane Kehrer(University Children's Hospital Tübingen), I. Krägeloh‐Mann(University Children's Hospital Tübingen), Andreas Dufke(University of Tübingen), Samuel Groeschel(University of Tübingen), Martin Kehrer(University of Tübingen)
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