Etiological heterogeneity of familial periventricular heterotopia and hydrocephalus-Reference-Cited by-同舟云学术

Etiological heterogeneity of familial periventricular heterotopia and hydrocephalus

Published:2004-08 Issue:5 Volume:26 Page:326-334
ISSN:0387-7604
Container-title:Brain and Development
language:en
Short-container-title:Brain and Development

Author:

Sheen Volney L,Basel-Vanagaite Lina,Goodman Jean R,Scheffer Ingrid E,Bodell Adria,Ganesh Vijay S,Ravenscroft Robert,Hill Robert S,Cherry Timothy J,Shugart Yin Y,Barkovich James,Straussberg Rachel,Walsh Christopher A

Publisher

Elsevier BV

Subject

Clinical Neurology,Developmental Neuroscience,General Medicine,Pediatrics, Perinatology, and Child Health

Reference25 articles.

1. Mutations in filamin 1 prevent migration of cerebral cortical neurons in human periventricular heterotopia;Fox;Neuron,1998

2. Mutations in the X-linked filamin 1 gene cause periventricular nodular heterotopia in males as well as in females;Sheen;Hum Mol Genet,2001

3. Familial periventricular heterotopia: missense and distal truncating mutations of the FLN1 gene;Moro;Neurology,2002

4. Bilateral periventricular nodular heterotopia with mental retardation and syndactyly in boys: a new X-linked mental retardation syndrome;Dobyns;Neurology,1997

5. Bilateral periventricular nodular heterotopia with mental retardation and frontonasal malformation;Guerrini;Neurology,1998

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