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Publications by B. A. Wicklow
Mutations in HYAL1, a Member of a Tandemly Distributed Multigene Family Encoding Disparate Hyaluronidase Activities, Cause a Newly Described Lysosomal Disorder, Mucopolysaccharidosis IX
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
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A Multigene Family Encoding Surface Glycoproteins in Trypanosoma Congolense
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Activating Mutations in PAK1, Encoding P21-Activated Kinase 1, Cause a Neurodevelopmental Disorder
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Mutations in a Member of the ADAMTS Gene Family Cause Thrombotic Thrombocytopenic Purpura
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Anomalous Placement of Introns in a Member of the Intermediate Filament Multigene Family: An Evolutionary Conundrum.
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a Newly Determined Member of the Meso -Diaminopimelate Dehydrogenase Family With a Broad Substrate Spectrum
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Mutations in RARS Cause a Hypomyelination Disorder Akin to Pelizaeus–Merzbacher Disease
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Mutations of IFT81, Encoding an IFT-B Core Protein, as a Rare Cause of a Ciliopathy
Cilia
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Isolation and cDNA Cloning of KSP-Cadherin, a Novel Kidney-Specific Member of the Cadherin Multigene Family
Journal of Biological Chemistry
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Mutations of POLR3A Encoding a Catalytic Subunit of RNA Polymerase Pol III Cause a Recessive Hypomyelinating Leukodystrophy
American Journal of Human Genetics
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