The spectrum ofZEB2mutations causing the Mowat-Wilson syndrome in Japanese populations

Dlx1&2-Dependent Expression of Zfhx1b (Sip1, Zeb2) Regulates the Fate Switch between Cortical and Striatal Interneurons

(2013) Gabriel L. McKinsey et al.   NEURON

The behavioral phenotype of Mowat-Wilson syndrome

(2012) Elizabeth Evans et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Characterization of the mutant β-subunit of β-hexosaminidase for dimer formation responsible for the adult form of Sandhoff disease with the motor neuron disease phenotype

(2012) Kenichiro Yamada et al.   JOURNAL OF BIOCHEMISTRY

Dual-Mode Modulation of Smad Signaling by Smad-Interacting Protein Sip1 Is Required for Myelination in the Central Nervous System

(2012) Qinjie Weng et al.   NEURON

Mowat-Wilson syndrome: Facial phenotype changing with age: Study of 19 Italian patients and review of the literature

(2009) L. Garavelli et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Sip1 regulates sequential fate decisions by feedback signaling from postmitotic neurons to progenitors

(2009) Eve Seuntjens et al.   NATURE NEUROSCIENCE

Recurrence of Mowat-Wilson syndrome in siblings with a novel mutation in theZEB2gene

(2008) Massimiliano Cecconi et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Atypical Mowat-Wilson patient confirms the importance of the novel association between ZFHX1B/SIP1 and NuRD corepressor complex

(2008) G. Verstappen et al.   HUMAN MOLECULAR GENETICS

Mowat-Wilson Syndrome Affecting 3 Siblings

(2008) Motoko Ohtsuka et al.   JOURNAL OF CHILD NEUROLOGY

The Jpred 3 secondary structure prediction server

(2008) C. Cole et al.   NUCLEIC ACIDS RESEARCH