(Q48267649)

English

The Thr124Met mutation in the peripheral myelin protein zero (MPZ) gene is associated with a clinically distinct Charcot-Marie-Tooth phenotype.

scientific article published in February 1999

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/10071056

The Thr124Met mutation in the peripheral myelin protein zero (MPZ) gene is associated with a clinically distinct Charcot-Marie-Tooth phenotype. (English)

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/10071056

1 reference

based on heuristic

inferred from title

Christine Van Broeckhoven

11

object named as

Van Broeckhoven C

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/10071056

author name string

De Jonghe P

1

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/10071056

Timmerman V

2

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/10071056

Ceuterick C

3

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/10071056

Nelis E

4

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/10071056

De Vriendt E

5

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/10071056

Löfgren A

6

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/10071056

Vercruyssen A

7

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/10071056

Verellen C

8

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/10071056

Van Maldergem L

9

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/10071056

Martin JJ

10

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/10071056

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publication date

1 February 1999

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/10071056

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/10071056

122 ( Pt 2)

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/10071056

281-290

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/10071056

Hereditary motor and sensory neuropathy with diaphragm and vocal cord paresis

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2F122.2.281

21 January 2018

Autosomal dominant Charcot-Marie-Tooth axonal neuropathy mapped on chromosome 7p (CMT2D).

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2F122.2.281

21 January 2018

Gene mapping in Gypsies identifies a novel demyelinating neuropathy on chromosome 8q24

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2F122.2.281

21 January 2018

Linkage and mutation analysis in an extended family with Charcot-Marie-Tooth disease type 1B.

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2F122.2.281

21 January 2018

Rapid screening of myelin genes in CMT1 patients by SSCP analysis: identification of new mutations and polymorphisms in the P0 gene

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2F122.2.281

21 January 2018

A locus for axonal motor-sensory neuropathy with deafness and mental retardation maps to Xq24-q26.

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2F122.2.281

21 January 2018

Mutations in the early growth response 2 (EGR2) gene are associated with hereditary myelinopathies

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2F122.2.281

21 January 2018

Localization of a Gene (CMT2A) for Autosomal Dominant Charcot-Marie-Tooth Disease Type 2 to Chromosome 1p and Evidence of Genetic Heterogeneity

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2F122.2.281

21 January 2018

Identifiers

10.1093/BRAIN/122.2.281

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/10071056

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/10071056

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