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Browsing by Author Gahl, William A.

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Epilepsy, ataxia, sensorineural deafness, tubulopathy, and KCNJ10 mutations

Author(s)Bockenhauer, Detlef; Feather, Sally; Stanescu, Horia C., et al
TypeJournal article
Date Published2009
Date Created-

Mistargeting of Peroxisomal EHHADH and Inherited Renal Fanconi's syndrome

Author(s)Klootwijk, Enriko D.; Reichold, Markus; Helip-Wooley, Amanda, et al
TypeJournal article
Date Published2014
Date Created-
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