DETECTION AND TREATMENT FOR CONGENITAL MUSCULAR DYSTROPHY WITH MITOCHONDRIAL DISORDER

PROBLEM TO BE SOLVED: To provide a method for detecting congenital muscular dystrophy with a mitochondrial disorder.SOLUTION: The method for detecting congenital muscular dystrophy with a mitochondrial disorder includes steps of: measuring variations of choline kinase β (CHKB) gene on the basis a sp...

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Bibliographische Detailangaben
Hauptverfasser: NISHINO KAZUMI, MIHASHI SATOMI
Format: Patent
Sprache:eng
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