Delineating the phenotypic spectrum of FOXG1 syndrome: from congenital microcephaly to hyperkinetic encephalopathy.

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VEGAS, Nancy, MAILLARD, Camille, BODDAERT, Nathalie, TOULOUSE, Joseph, SCHAEFER, Elise, LERMAN-SAGIE, Tally, LEV, Dorit, MAGALIE, Barth, MOUTTON, Sébastien, HAAN, Eric, ISIDOR, Bertrand, HERON, Delphine, MILH, Mathieu, RONDEAU, Stéphane, MICHOT, Caroline, VALENCE, Stephanie, WAGNER, Sabrina, HULLY, Marie, MIGNOT, Cyril, MASUREL, Alice, DATTA, Alexandre, ODENT, Sylvie, NIZON, Mathilde, LAZARO, Leila, VINCENT, Marie, COGNÉ, Benjamin, GUERROT, Anne Marie, ARPIN, Stéphanie, PEDESPAN, Jean Michel, CAUBEL, Isabelle, PONTIER, Benedicte, TROUDE, Baptiste, RIVIER, Francois, PHILIPPE, Christophe, BIENVENU, Thierry, SPITZ, Marie-Aude, BERY, Amandine et BAHI-BUISSON, Nadia, 2018. Delineating the phenotypic spectrum of FOXG1 syndrome: from congenital microcephaly to hyperkinetic encephalopathy.: From congenital microcephaly to hyperkinetic encephalopathy. Neurology Genetics. 7 novembre 2018. Vol. 4, n° 6pp. e281. DOI 10.1212/NXG.0000000000000281.