Pages that link to "Q74331659"
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The following pages link to Sarcoglycanopathies in Dutch patients with autosomal recessive limb girdle muscular dystrophy (Q74331659):
Displaying 10 items.
- Costameric proteins in human skeletal muscle during muscular inactivity (Q28283040) (← links)
- Prevalence of genetic muscle disease in Northern England: in-depth analysis of a muscle clinic population (Q33685609) (← links)
- Rescue of sarcoglycan mutations by inhibition of endoplasmic reticulum quality control is associated with minimal structural modifications (Q34233835) (← links)
- Sarcoglycan complex in masseter and sternocleidomastoid muscles of baboons: an immunohistochemical study (Q35856467) (← links)
- Somatic mosaicism of a point mutation in the dystrophin gene in a patient presenting with an asymmetrical muscle weakness and contractures. (Q54764281) (← links)
- Impact of PYROXD1 deficiency on cellular respiration and correlations with genetic analyses of limb-girdle muscular dystrophy in Saudi Arabia and Sudan (Q57788875) (← links)
- Clinical and genetic spectrum of sarcoglycanopathies in a large cohort of Chinese patients (Q64245758) (← links)
- LGMD2E patients risk developing dilated cardiomyopathy (Q73685043) (← links)
- In tandem analysis of CLCN1 and SCN4A greatly enhances mutation detection in families with non-dystrophic myotonia (Q80863131) (← links)
- Combined Use of CFTR Correctors in LGMD2D Myotubes Improves Sarcoglycan Complex Recovery (Q90189339) (← links)