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A Peroxisomal Disorder of Severe Intellectual Disability, Epilepsy, and Cataracts Due to Fatty Acyl-CoA Reductase 1 Deficiency
Author(s):
Rebecca Buchert
,
Hasan Tawamie
,
Steven Smith
,
Steffen Uebe
,
A Innes
,
Bassam Al Hallak
,
Arif B. Ekici
,
Heinrich Sticht
,
Bernd Schwarze
,
Ryan Lamont
,
Jillian Parboosingh
,
Francois Bernier
,
Rami Abou Jamra
Publication date:
2014-11-01
Journal:
The American Journal of Human Genetics
Publisher:
Elsevier BV
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Journal of Disability Research
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DOI::
10.1016/j.ajhg.2014.10.003
License:
https://www.elsevier.com/tdm/userlicense/1.0/
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