Associated Papers
TCAP gene is not a common cause of cardiomyopathy in Iranian patients.
Alaei Z et al.
European Journal of Medical Research, 2023
The clinical features and TCAP mutation spectrum in a Chinese cohort of patients with limb-girdle muscular dystrophy R7.
Lv X et al.
Human Molecular Genetics, 2023
Unique Clinical, Radiological and Histopathological Characteristics of a Southeast Asian Cohort of Patients with Limb-Girdle Muscular Dystrophy 2G/LGMD-R7-Telethonin-Related.
Chen Z et al.
Journal of Neuromuscular Diseases, 2023
Phenotypic Spectrum of Myopathies with Recessive Anoctamin-5 Mutations.
Vázquez J et al.
Journal of Neuromuscular Diseases, 2020
Novel mutation in TCAP manifesting with asymmetric calves and early-onset joint retractions.
de Fuenmayor-Fernández de la Hoz CP et al.
Neuromuscular Disorders : Nmd, 2016
Limb-girdle muscular dystrophies: where next after six decades from the first proposal (Review).
Mahmood OA et al.
Molecular Medicine Reports, 2014
Telethonin-deficiency initially presenting as a congenital muscular dystrophy.
Ferreiro A et al.
Neuromuscular Disorders : Nmd, 2011
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