Published in
Lippincott, Williams & Wilkins, Neurology: Genetics, 6(2), p. e114, 2016
DOI: 10.1212/nxg.0000000000000114
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Heterozygous mutations in HSD17B4 cause juvenile peroxisomal D-bifunctional protein deficiency
Journal article published in 2016 by
David J. Amor,
Ashley Pl L. Marsh,
Elsdon Storey,
Rick Tankard 
,
Greta Gillies,
Martin B. Delatycki,
Kate Pope,
Catherine Bromhead,
Richard J. Leventer,
Melanie Bahlo,
Paul J. Lockhart
,
Greta Gillies,
Martin B. Delatycki,
Kate Pope,
Catherine Bromhead,
Richard J. Leventer,
Melanie Bahlo,
Paul J. Lockhart
This paper is made freely available by the publisher.
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