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Pazour, Gregory

One or more keywords matched the following items that are connected to Pazour, Gregory

Item Type	Name
Academic Article	Combined NGS approaches identify mutations in the intraflagellar transport gene IFT140 in skeletal ciliopathies with early progressive kidney Disease.
Academic Article	Disruption of Mks1 localization to the mother centriole causes cilia defects and developmental malformations in Meckel-Gruber syndrome.
Concept	Retinitis Pigmentosa
Academic Article	Fifteen years of research on oral-facial-digital syndromes: from 1 to 16 causal genes.
Academic Article	A global analysis of IFT-A function reveals specialization for transport of membrane-associated proteins into cilia.

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