Mutation update for the SATB2 gene

Zarate, YA; Bosanko, KA; Caffrey, AR; Bernstein, JA; Martin, DM; Williams, MS; Berry-Kravis, EM; Mark, PR; Manning, MA; Bhambhani, V; Vargas, M; Seeley, AH; Estrada-Veras, JI; vanDooren, MF; Schwab, M; Vanderver, A; Melis, D; Alsadah, A; Sadler, L; V

Zarate, YA (reprint author), Arkansas Childrens Hosp, 1 Childrens Way,Slot 512-22, Little Rock, AR 72202 USA.

HUMAN MUTATION, 2019; 40 (8): 1013

Abstract

SATB2-associated syndrome (SAS) is an autosomal dominant neurodevelopmental disorder caused by alterations in the SATB2 gene. Here we present a review......

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