Mutations in the phospholipid remodeling gene SERAC1 cause MEGDEL syndrome.
Identifieur interne : 000D02 ( Main/Exploration ); précédent : 000D01; suivant : 000D03Mutations in the phospholipid remodeling gene SERAC1 cause MEGDEL syndrome.
Auteurs : Athanasia Alexoudi ; Susanne A. SchneiderSource :
- Movement disorders : official journal of the Movement Disorder Society [ 1531-8257 ] ; 2012.
PubMed: 23401890
Affiliations:
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Le document en format XML
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