(Q41104677)

26 September 2017

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title

Nondystrophinopathic muscular dystrophies including myotonic dystrophy (English)

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26 September 2017

Nonaka I

1

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26 September 2017

Kobayashi O

series ordinal

2

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26 September 2017

Osari S

series ordinal

3

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26 September 2017

publication date

1 June 1996

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Seminars in pediatric neurology

26 September 2017

published in

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26 September 2017

volume

3

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26 September 2017

issue

2

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26 September 2017

page(s)

110-121

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Unusual type of benign x-linked muscular dystrophy

26 September 2017

cites work

1 reference

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7 January 2021

Identification of a novel X-linked gene responsible for Emery-Dreifuss muscular dystrophy

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7 January 2021

Emery-dreifuss muscular dystrophy

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7 January 2021

Emery-Dreifuss syndrome

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7 January 2021

On the classification, natural history and treatment of the myopathies.

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7 January 2021

Mapping of a chromosome 15 region involved in limb girdle muscular dystrophy.

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7 January 2021

A primary expression map of the chromosome 15q15 region containing the recessive form of limb-girdle muscular dystrophy (LGMD2A) gene.

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7 January 2021

Mutations in the proteolytic enzyme calpain 3 cause limb-girdle muscular dystrophy type 2A

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7 January 2021

A gene for autosomal recessive limb-girdle muscular dystrophy maps to chromosome 2p

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7 January 2021

Limb-girdle muscular dystrophy: clinical and pathologic reevaluation

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7 January 2021

Dystrophin-associated proteins in muscular dystrophy

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7 January 2021

Deficiency of the 50K dystrophin-associated glycoprotein in severe childhood autosomal recessive muscular dystrophy

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7 January 2021

Severe childhood muscular dystrophy affecting both sexes and frequent in Tunisia

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7 January 2021

Missense mutations in the adhalin gene linked to autosomal recessive muscular dystrophy

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7 January 2021

Severe childhood autosomal recessive muscular dystrophy with the deficiency of the 50 kDa dystrophin-associated glycoprotein maps to chromosome 13q12

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7 January 2021

Localization of a gene for Fukuyama type congenital muscular dystrophy to chromosome 9q31-33

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7 January 2021

Congenital progressive muscular dystrophy of the Fukuyama type - clinical, genetic and pathological considerations

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7 January 2021

Muscle histochemistry in congenital muscular dystrophy with central nervous system involvement

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7 January 2021

Abnormal localization of laminin subunits in muscular dystrophies

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7 January 2021

Clinical phenotype in congenital muscular dystrophy: correlation with expression of merosin in skeletal

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7 January 2021

Expression of laminin subunits in congenital muscular dystrophy

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7 January 2021

Congenital muscular dystrophy: Clinical and pathologic study of 50 patients with the classical (Occidental) merosin-positive form

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7 January 2021

Basement membrane abnormality in merosin-negative congenital muscular dystrophy

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7 January 2021

Localization of merosin-negative congenital muscular dystrophy to chromosome 6q2 by homozygosity mapping

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7 January 2021

Autosomal recessive distal muscular dystrophy as a new type of progressive muscular dystrophy. Seventeen cases in eight families including an autopsied case

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7 January 2021

Linkage of Miyoshi myopathy (distal autosomal recessive muscular dystrophy) locus to chromosome 2p12-14

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7 January 2021

Autosomal recessive distal muscular dystrophy: a comparative study with distal myopathy with rimmed vacuole formation

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7 January 2021

Autosomal recessive distal muscular dystrophy: normal expression of dystrophin, utrophin and dystrophin-associated proteins in muscle fibers

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7 January 2021

Location of facioscapulohumeral muscular dystrophy gene on chromosome 4.

1 reference

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7 January 2021

Chromosome 4q DNA rearrangements associated with facioscapulohumeral muscular dystrophy

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7 January 2021

Inflammatory response in facioscapulohumeral muscular dystrophy (FSHD): immunocytochemical and genetic analyses

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7 January 2021

Expansion of an unstable DNA region and phenotypic variation in myotonic dystrophy

1 reference

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7 January 2021

An unstable triplet repeat in a gene related to myotonic muscular dystrophy

1 reference

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7 January 2021

Unstable DNA sequence in myotonic dystrophy

1 reference

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7 January 2021

Correlation between CTG trinucleotide repeat length and frequency of severe congenital myotonic dystrophy

1 reference

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7 January 2021

Beta-sarcoglycan (A3b) mutations cause autosomal recessive muscular dystrophy with loss of the sarcoglycan complex

1 reference

https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980040-4

7 January 2021

β–sarcoglycan: characterization and role in limb–girdle muscular dystrophy linked to 4q12

1 reference

https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980040-4

7 January 2021

Mutations in the dystrophin-associated protein gamma-sarcoglycan in chromosome 13 muscular dystrophy

1 reference

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7 January 2021

10.1016/S1071-9091(96)80040-4

Identifiers

DOI

1 reference

26 September 2017

1 reference