Novel mutations in LMNA A/C gene and associated phenotypes.

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Management of cardiac involvement in muscular dystrophies: paediatric versus adult forms

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Novel mutations in LMNA A/C gene and associated phenotypes.

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Novel mutations in LMNA A/C gene and associated phenotypes.

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Novel mutations in LMNA A/C gene and associated phenotypes.

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Novel mutations in LMNA A/C gene and associated phenotypes.

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P1476

Novel mutations in LMNA A/C gene and associated phenotypes.

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Alessandro Testori

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Annalaura Torella

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Antonella Taglia

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Esther Picillo

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Gerardo Nigro

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Giulio Piluso

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Luisa Politano

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Manuela Ergoli

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Paola D'Ambrosio

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Roberta Petillo

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P2860

Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy

Mandibuloacral dysplasia is caused by a mutation in LMNA-encoding lamin A/C

Overlapping syndromes in laminopathies: a meta-analysis of the reported literature

Missense mutations in the rod domain of the lamin A/C gene as causes of dilated cardiomyopathy and conduction-system disease

Identification of mutations in the gene encoding lamins A/C in autosomal dominant limb girdle muscular dystrophy with atrioventricular conduction disturbances (LGMD1B)

Recurrent de novo point mutations in lamin A cause Hutchinson-Gilford progeria syndrome

LMNA mutations in atypical Werner's syndrome

The laminopathies: a clinical review

[Arrhythmia and muscular exercise intolerance revealing lamin genetic defect in a young adult].

[Case with Emery-Dreifuss muscular dystrophy diagnosed forty-two years after onset and implanted with a cardiac resynchronization therapy defibrillator].

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116-119

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2-3

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2015-12-01T00:00:00Z

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27199538

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4859074

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Novel mutations in LMNA A/C gene and associated phenotypes.

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P2860

P2860

Novel mutations in LMNA A/C gene and associated phenotypes.

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