(Q54525761)

English

Novel B4GALNT1 mutations in a complicated form of hereditary spastic paraplegia.

scientific article

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

30 May 2018

http://europepmc.org/abstract/MED/24283893

Novel B4GALNT1 mutations in a complicated form of hereditary spastic paraplegia. (English)

1 reference

Europe PubMed Central

PubMed publication ID

30 May 2018

http://europepmc.org/abstract/MED/24283893

author name string

S M Wakil

1

1 reference

Europe PubMed Central

PubMed publication ID

30 May 2018

http://europepmc.org/abstract/MED/24283893

D M Monies

2

1 reference

Europe PubMed Central

PubMed publication ID

30 May 2018

http://europepmc.org/abstract/MED/24283893

K Ramzan

3

1 reference

Europe PubMed Central

PubMed publication ID

30 May 2018

http://europepmc.org/abstract/MED/24283893

S Hagos

4

1 reference

Europe PubMed Central

PubMed publication ID

30 May 2018

http://europepmc.org/abstract/MED/24283893

L Bastaki

5

1 reference

Europe PubMed Central

PubMed publication ID

30 May 2018

http://europepmc.org/abstract/MED/24283893

B F Meyer

6

1 reference

Europe PubMed Central

PubMed publication ID

30 May 2018

http://europepmc.org/abstract/MED/24283893

S Bohlega

7

1 reference

Europe PubMed Central

PubMed publication ID

30 May 2018

http://europepmc.org/abstract/MED/24283893

publication date

27 November 2013

1 reference

Europe PubMed Central

PubMed publication ID

30 May 2018

http://europepmc.org/abstract/MED/24283893

Clinical Genetics

1 reference

Europe PubMed Central

PubMed publication ID

30 May 2018

http://europepmc.org/abstract/MED/24283893

86

1 reference

Europe PubMed Central

PubMed publication ID

30 May 2018

http://europepmc.org/abstract/MED/24283893

5

1 reference

Europe PubMed Central

PubMed publication ID

30 May 2018

http://europepmc.org/abstract/MED/24283893

500-501

1 reference

Europe PubMed Central

PubMed publication ID

30 May 2018

http://europepmc.org/abstract/MED/24283893

Recent advances in the genetics of spastic paraplegias

1 reference

https://api.crossref.org/works/10.1111%2FCGE.12312

21 January 2018

A new locus for autosomal recessive complicated hereditary spastic paraplegia (SPG26) maps to chromosome 12p11.1-12q14.

1 reference

https://api.crossref.org/works/10.1111%2FCGE.12312

21 January 2018

Infantile-onset symptomatic epilepsy syndrome caused by a homozygous loss-of-function mutation of GM3 synthase.

1 reference

https://api.crossref.org/works/10.1111%2FCGE.12312

21 January 2018

Alteration of ganglioside biosynthesis responsible for complex hereditary spastic paraplegia

1 reference

https://api.crossref.org/works/10.1111%2FCGE.12312

21 January 2018

Identifiers

10.1111/CGE.12312

1 reference

Europe PubMed Central

PubMed publication ID

30 May 2018

http://europepmc.org/abstract/MED/24283893

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

30 May 2018

http://europepmc.org/abstract/MED/24283893

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