4th Workshop of the European CMT-Consortium--62nd ENMC International Workshop: rare forms of Charcot-Marie-Tooth disease and related disorders 16-18 October 1998, Soestduinen, The Netherlands (Q77982677)

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scientific article published on 01 June 1999

Language	Label	Description	Also known as
English	4th Workshop of the European CMT-Consortium--62nd ENMC International Workshop: rare forms of Charcot-Marie-Tooth disease and related disorders 16-18 October 1998, Soestduinen, The Netherlands	scientific article published on 01 June 1999

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scholarly article

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10399758%20AND%20SRC:MED&resulttype=core&format=json

9 December 2019

4th Workshop of the European CMT-Consortium--62nd ENMC International Workshop: rare forms of Charcot-Marie-Tooth disease and related disorders 16-18 October 1998, Soestduinen, The Netherlands (English)

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10399758%20AND%20SRC:MED&resulttype=core&format=json

9 December 2019

publication date

1 June 1999

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9 December 2019

Neuromuscular Disorders

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9 December 2019

9

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9 December 2019

4

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9 December 2019

279-287

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9 December 2019

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

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Correlation between the histopathologic, genotypic, and phenotypic features of hereditary peripheral neuropathies in childhood

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Autosomal recessive motor and sensory neuropathy with excessive myelin outfolding

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Two divergent types of nerve pathology in patients with different P0 mutations in Charcot-Marie-Tooth disease

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Dominantly inherited motor and sensory neuropathy with excessive myelin folding complex

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Autosomal recessive form of hereditary motor and sensory neuropathy type I.

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Homozygosity mapping of an autosomal recessive form of demyelinating Charcot-Marie-Tooth disease to chromosome 5q23-q33.

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A clinical, electrophysiologic, neuropathologic, and genetic study of two large Algerian families with an autosomal recessive demyelinating form of Charcot-Marie-Tooth disease

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A YAC contig of approximately 3 Mb from human chromosome 5q31-->q33.

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Autosomal recessive hereditary motor and sensory neuropathy with focally folded myelin sheaths: clinical, electrophysiologic, and genetic aspects of a large family.

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Hereditary neuralgic amyotrophy: evidence for genetic homogeneity and mapping to chromosome 17q25

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An STS-based radiation hybrid map of the human genome

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Identifiers

10.1016/S0960-8966(99)00017-6

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10399758%20AND%20SRC:MED&resulttype=core&format=json

9 December 2019

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10399758%20AND%20SRC:MED&resulttype=core&format=json

9 December 2019

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