Pseudometabolic presentation of dystrophinopathy due to a missense mutation

Author:

Veerapandiyan Aravindhan,Shashi Vandana,Jiang Yong-Hui,Gallentine William Brian,Schoch Kelly,Smith Edward Clinton

Publisher

Wiley

Subject

Physiology (medical),Cellular and Molecular Neuroscience,Neurology (clinical),Physiology

Reference41 articles.

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2. Elevation of serum creatine kinase as the only manifestation of an intragenic deletion of the dystrophin gene in three unrelated families;Melis;Eur J Paediatr Neurol,1998

3. Asymptomatic dystrophinopathy;Morrone;Am J Med Genet,1997

4. Becker muscular dystrophy with marked divergence between clinical and molecular genetic findings: case series;Ramelli;Swiss Med Wkly,2006

5. Dystrophin abnormalities in Duchenne/Becker muscular dystrophy;Hoffman;Neuron,1989

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