Mapping of a new locus for autosomal recessive demyelinating Charcot-Marie-Tooth disease to 19q13.1-13.3 in a large consanguineous Lebanese family: exclusion of MAG as a candidate gene.
about
Periaxin mutations cause recessive Dejerine-Sottas neuropathy.Mutation in WNT10A is associated with an autosomal recessive ectodermal dysplasia: the odonto-onycho-dermal dysplasiaMutations in MTMR13, a new pseudophosphatase homologue of MTMR2 and Sbf1, in two families with an autosomal recessive demyelinating form of Charcot-Marie-Tooth disease associated with early-onset glaucomaMutations in FGD4 encoding the Rho GDP/GTP exchange factor FRABIN cause autosomal recessive Charcot-Marie-Tooth type 4HA second locus for an axonal form of autosomal recessive Charcot-Marie-Tooth disease maps to chromosome 19q13.3.Deciphering peripheral nerve myelination by using Schwann cell expression profiling.Periaxin mutations cause a broad spectrum of demyelinating neuropathies.A novel locus for autosomal recessive peripheral neuropathy in the EGR2 region on 10q23.A review of the diverse genetic disorders in the Lebanese population: highlighting the urgency for community genetic services.Dejerine-Sottas disease and hereditary demyelinating polyneuropathy of infancy.Autosomal-recessive forms of demyelinating Charcot-Marie-Tooth disease.Molecular genetics of autosomal-recessive axonal Charcot-Marie-Tooth neuropathies.Biological role of dystroglycan in Schwann cell function and its implications in peripheral nervous system diseases.Demyelinating prenatal and infantile developmental neuropathies.Autosomal recessive Charcot-Marie-Tooth disease: from genes to phenotypes.[Genetics of neuropathies].Nerve Biopsy Is Still Useful in Some Inherited Neuropathies.Nerve conduction abnormalities in aging mice deficient for myelin-associated glycoprotein.Hereditary motor and sensory neuropathy-russe: New autosomal recessive neuropathy in balkan gypsies
P2860
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P2860
Mapping of a new locus for autosomal recessive demyelinating Charcot-Marie-Tooth disease to 19q13.1-13.3 in a large consanguineous Lebanese family: exclusion of MAG as a candidate gene.
description
2000 nî lūn-bûn
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2000 թուականի Յունիսին հրատարակուած գիտական յօդուած
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2000 թվականի հունիսին հրատարակված գիտական հոդված
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2000年の論文
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2000年論文
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2000年論文
@zh-hant
2000年論文
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2000年論文
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2000年論文
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2000年论文
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name
Mapping of a new locus for aut ...... ion of MAG as a candidate gene
@nl
Mapping of a new locus for aut ...... on of MAG as a candidate gene.
@ast
Mapping of a new locus for aut ...... on of MAG as a candidate gene.
@en
type
label
Mapping of a new locus for aut ...... ion of MAG as a candidate gene
@nl
Mapping of a new locus for aut ...... on of MAG as a candidate gene.
@ast
Mapping of a new locus for aut ...... on of MAG as a candidate gene.
@en
prefLabel
Mapping of a new locus for aut ...... ion of MAG as a candidate gene
@nl
Mapping of a new locus for aut ...... on of MAG as a candidate gene.
@ast
Mapping of a new locus for aut ...... on of MAG as a candidate gene.
@en
P2093
P2860
P356
P1476
Mapping of a new locus for aut ...... ion of MAG as a candidate gene
@en
P2093
Bouvagnet P
Claustres M
Loiselet J
Maisonobe T
Mégarbané A
P2860
P304
P356
10.1086/302980
P407
P577
2000-06-02T00:00:00Z