(Q50924723)

25 March 2018

title

Duplication of proteolipid protein gene: a possible major cause of Pelizaeus-Merzbacher disease. (English)

1 reference

25 March 2018

author

Wuh-liang Hwu

2

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25 March 2018

Wang-Tso Lee

3

1 reference

25 March 2018

author name string

Wang PJ

1

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25 March 2018

Wang TR

4

1 reference

25 March 2018

Shen YZ

5

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25 March 2018

publication date

1 September 1997

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25 March 2018

published in

Pediatric Neurology

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25 March 2018

volume

17

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25 March 2018

issue

2

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25 March 2018

page(s)

125-128

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25 March 2018

An interstitial duplication of the X chromosome in a male allows physical fine mapping of probes from the Xq13-q22 region

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2897%2900088-X

7 January 2021

The gene encoding for the major brain proteolipid (PLP) maps on the q-22 band of the human X chromosome

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2897%2900088-X

7 January 2021

DM20 mRNA splice product of the myelin proteolipid protein gene is expressed in the murine heart

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2897%2900088-X

7 January 2021

A new mutation in the proteolipid protein (PLP) gene in a German family with pelizaeus-merzbacher disease

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2897%2900088-X

7 January 2021

In-frame deletion in the proteolipid protein gene of a family with Pelizaeus-Merzbacher disease

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2897%2900088-X

7 January 2021

Proteolipid protein gene dosage effect in Pelizaeus-Merzbacher disease

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2897%2900088-X

7 January 2021

Overexpression of DM20 messenger RNA in two brothers with Pelizaeus-Merzbacher disease

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2897%2900088-X

7 January 2021

Neurophysiologic studies and MRI in Pelizaeus-Merzbacher disease: comparison of classic and connatal forms

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2897%2900088-X

7 January 2021

Glucose-6-phosphatase gene G327A mutation is common in Chinese patients with glycogen storage disease type Ia

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2897%2900088-X

7 January 2021

Premature arrest of myelin formation in transgenic mice with increased proteolipid protein gene dosage

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2897%2900088-X

7 January 2021

Glial cell degeneration and hypomyelination caused by overexpression of myelin proteolipid protein gene

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2897%2900088-X

7 January 2021

The peripheral myelin protein gene PMP-22 is contained within the Charcot-Marie-Tooth disease type 1A duplication

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2897%2900088-X

7 January 2021

Detection of deletion within 17p11.2 in 7 French families with hereditary neuropathy with liability to pressure palsies (HNPP)

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2897%2900088-X

7 January 2021

10.1016/S0887-8994(97)00088-X

Identifiers

DOI

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25 March 2018

PubMed ID

9367291

1 reference

25 March 2018