Paul Lockhart
Murdoch Childrens Research Institute
15 papers found
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Ectopic HCN4 Provides a Target Biomarker for the Genetic Spectrum of mTORopathies
Download from doi.orgThe clinical, imaging, pathological and genetic landscape of bottom-of-sulcus dysplasia
UploadIntrinsic and secondary epileptogenicity in focal cortical dysplasia type II
Download from onlinelibrary.wiley.comDroplet digital PCR as a first-tier molecular diagnostic tool for focal cortical dysplasia type II
Download from academic.oup.comHeterozygous PNPT1 Variants Cause Spinocerebellar Ataxia Type 25
UploadASK1 is a novel molecular target for preventing aminoglycoside-induced hair cell death
UploadA family study implicates GBE1 in the etiology of autism spectrum disorder
UploadMutations in DCC cause isolated agenesis of the corpus callosum with incomplete penetrance
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