(Q39038032)

8 September 2017

title

Complicated hereditary spastic paraparesis with cerebral white matter lesions (English)

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8 September 2017

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Gutmann DH

1

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8 September 2017

Fischbeck KH

series ordinal

2

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8 September 2017

Kamholz J

series ordinal

3

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8 September 2017

publication date

1 June 1990

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American Journal of Medical Genetics Part A

8 September 2017

published in

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8 September 2017

volume

36

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8 September 2017

issue

2

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8 September 2017

page(s)

251-257

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A familial syndrome of infantile optic atrophy, movement disorder, and spastic paraplegia

8 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.1320360222

The Troyer syndrome. A recessive form of spastic paraplegia with distal muscle wasting

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.1320360222

The mast syndrome. A recessively inherited form of presenile dementia with motor disturbances

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.1320360222

Familial Spastic Paraplegia with Amyotrophy, Oligophrenia, and Central Retinal Degeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.1320360222

Familial spastic paraparesis: an adrenoleukodystrophy phenotype?

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.1320360222

Familial spastic paraparesis and deafness. A new x-linked neurodegenerative disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.1320360222

21 January 2018

Identifiers

DOI

10.1002/AJMG.1320360222

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8 September 2017

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