(Q42474774)

1 November 2017

title

Unusual variants of Alexander's disease (English)

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13

Frederik Barkhof

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1 November 2017

9

Bruce Cree

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1 November 2017

author name string

Marjo S van der Knaap

1

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1 November 2017

Gajja S Salomons

2

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Rong Li

3

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Emilio Franzoni

4

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1 November 2017

Luiz González Gutiérrez-Solana

5

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Leo M E Smit

6

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Richard Robinson

7

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Collin D Ferrie

8

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Alyssa Reddy

10

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Neil Thomas

11

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Brenda Banwell

12

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Cornelis Jakobs

14

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Anne Johnson

15

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Albee Messing

16

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Michael Brenner

17

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publication date

1 March 2005

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volume

57

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1 November 2017

issue

3

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1 November 2017

page(s)

327-338

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Mutations in GFAP, encoding glial fibrillary acidic protein, are associated with Alexander disease

1 November 2017

cites work

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GFAP mutations in Alexander disease

21 January 2018

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Infantile Alexander disease: spectrum of GFAP mutations and genotype-phenotype correlation

21 January 2018

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Nomenclature for the description of human sequence variations.

21 January 2018

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A novel mutation in glial fibrillary acidic protein gene in a patient with Alexander disease

21 January 2018

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Diagnosis of Alexander disease in a Japanese patient by molecular genetic analysis.

21 January 2018

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Atypical focal MRI lesions in a case of juvenile Alexander's disease

21 January 2018

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Identification of GFAP gene mutation in hereditary adult-onset Alexander's disease

21 January 2018

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Autosomal dominant palatal myoclonus and spinal cord atrophy

21 January 2018

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Adult Alexander disease with autosomal dominant transmission: a distinct entity caused by mutation in the glial fibrillary acid protein gene.

21 January 2018

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21 January 2018

Identifiers

DOI

10.1002/ANA.20381

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1 November 2017

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