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Clinical, pathological, and genetic features of limb-girdle muscular dystrophy type 2A with new calpain 3 gene mutations in seven patients from three Japanese families
by
Kawai, Hisaomi
,
Akaike, Masashi
,
Kunishige, Makoto
,
Inui, Toshio
,
Adachi, Katsuhito
,
Kimura, Chiyomi
,
Kawajiri, Masakazu
,
Nishida, Yoshihiko
,
Endo, Itsuro
,
Kashiwagi, Setsuko
,
Nishino, Hiroshi
,
Fujiwara, Tsutomu
,
Okuno, Shiro
,
Roudaut, Carinne
,
Richard, Isabelle
,
Beckmann, Jacques S.
,
Miyoshi, Kazuo
,
Matsumoto, Toshio
Published in
Muscle & nerve
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PS-19-5 Relation between skull hyperostosis and abnormal expansion of myotonin-protein kinase gene in myotonic dystrophy
by
Inui, Toshio
,
Kashiwagi, Setsuko
,
Kimura, Chiyomi
,
Yamagata, Hidehisa
,
Miki, Tetsuro
,
Kawai, Hisaomi
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Electroencephalography and clinical neurophysiology / electromyography and motor control
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Electroencephalography And Clinical Neurophysiology / Electromyography And Motor Control
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Muscle & Nerve
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Age Of Onset
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Biological And Medical Sciences
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Biopsy
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Calpain - Genetics
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Calpain 3 Gene
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Child
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Clinical Feature
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Clinical Neurology
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Diseases Of Striated Muscles. Neuromuscular Diseases
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Dna Mutational Analysis
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Exons
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Family Health
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Female
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Haplotypes
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Humans
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Isoenzymes - Genetics
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Japan
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Life Sciences & Biomedicine
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Limb-Girdle Muscular Dystrophy Type 2A
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Limb‐Girdle Muscular Dystrophy Type 2A
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Wiley-Blackwell Journals (Backfile Content)
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Sciencedirect®
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Sciencedirect Freedom Collection
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Wiley-Blackwell Read & Publish Collection
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