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Household transmission of haemolytic uraemic syndrome associated with Escherichia coli O104:H4, south-western France, June 2011.

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Association of a homozygous (TA)8 promoter polymorphism and a N400D mutation of UGT1A1 in a child with Crigler‐Najjar type II syndrome

P. Labrune, A. Myara, J. Francoual, 2002, Human mutation.

Crigler‐Najjar syndrome type I in Tunisia may be associated with a founder effect related to the Q357R mutation within the UGT1 gene

F. Gottrand, P. Labrune, A. Myara, 2002, Human mutation.

CONCENTRATIONS OF APOLIPOPROTEINS E, C2 AND C3 AND LIPID PROFILE IN PREECLAMPSIA

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