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List of works by K B Leydiker

A homozygous mutation in KCTD7 links neuronal ceroid lipofuscinosis to the ubiquitin-proteasome system.

scientific article

Biochemical, molecular, and clinical characteristics of children with short chain acyl-CoA dehydrogenase deficiency detected by newborn screening in California ⬇️

scientific article published on February 9, 2012

Maternal medium-chain acyl-CoA dehydrogenase deficiency identified by newborn screening.

scientific article

Reduction in newborn screening metabolic false-positive results following a new collection protocol.

scientific article published on 31 October 2013

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