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Neurocognitive and neuropsychiatric phenotypes associated with the mutation L238Q of the α-L-iduronidase gene in Hurler–Scheie syndrome

✍ Scribed by Ahmed, Alia; Whitley, Chester B.; Cooksley, Renee; Rudser, Kyle; Cagle, Stephanie; Ali, Nadia; Delaney, Kathleen; Yund, Brianna; Shapiro, Elsa


Book ID
122166892
Publisher
Elsevier Science
Year
2014
Tongue
English
Weight
308 KB
Volume
111
Category
Article
ISSN
1096-7192

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