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Functional and electrophysiological characterization of four non-truncating mutations responsible for creatine transporter (SLC6A8) deficiency syndrome. [electronic resource] by
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- Salomons, Gajja S
- Mellot-Draznieks, Caroline
- Brulé, Emilie
- de Lonlay, Pascale
- Toulhoat, Hervé
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In:
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A mouse model for creatine transporter deficiency reveals early onset cognitive impairment and neuropathology associated with brain aging. [electronic resource] by
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- Napoli, Debora
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In:
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- Aoi, Noriko
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Clinical biochemistry vol. 44
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Creatine Transporter Deficiency: Screening of Males with Neurodevelopmental Disorders and Neurocognitive Characterization of a Case. [electronic resource] by
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- Rennert, Owen
- Jiang, Susanqi
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- Pasquali, Marzia
- Swedo, Susan
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- Carrillo, Nuria
Producer: 20171208
In:
Journal of developmental and behavioral pediatrics : JDBP vol. 37
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Dodecyl creatine ester-loaded nanoemulsion as a promising therapy for creatine transporter deficiency. [electronic resource] by
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- Miles, Keila N
- Costa, Narciso
- Taran, Frédéric
- Pruvost, Alain
- Benoit, Jean-Pierre
- Skelton, Matthew R
- Lonlay, Pascale de
- Mabondzo, Aloïse
Producer: 20200608
In:
Nanomedicine (London, England) vol. 14
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