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1036 Gracile Syndrome in a Turkish Newborn Infant Caused by a Homozygous Mutation (P99L) in Complex Iii Assembly Factor BCS1L
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Serdaroglu E, Takci S, Kotarsky H, et al
1036 Gracile Syndrome in a Turkish Newborn Infant Caused by a Homozygous Mutation (P99L) in Complex Iii Assembly Factor BCS1L
Archives of Disease in Childhood 2012;97:A297.

Publication history

  • First published October 1, 2012.
Online issue publication 
March 22, 2016

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© 2012, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions.