A novel mitochondrial DNA deletion in a patient with Kearns-Sayre syndrome: A late-onset of the fatal cardiac conduction deficit and cardiomyopathy accompanying long-term rGH treatment

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A novel mitochondrial DNA deletion in a patient with Kearns-Sayre syndrome: A late-onset of the fatal cardiac conduction deficit and cardiomyopathy accompanying long-term rGH treatment

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: Kearns-Sayre Syndrome (KSS) is a multisystem disorder caused by a dysfunction of the oxidative phosphorylation system within mitochondria. Mitochondrial DNA (mtDNA) rearrangements are a key molecular feature of this disease, which manifest a broad phenotypic spectrum. | A novel mitochondrial DNA deletion in a patient with Kearns-Sayre syndrome: A late-onset of the fatal cardiac conduction deficit and cardiomyopathy accompanying long-term rGH treatment

Đang chuẩn bị liên kết để tải về tài liệu:
A novel mitochondrial DNA deletion in a patient with Kearns-Sayre syndrome: A late-onset of the fatal cardiac conduction deficit and cardiomyopathy accompanying long-term rGH treatment

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Severe clinical manifestation of mitochondrial 3-hydroxy-3-methylglutarylCoA synthase deficiency associated with two novel mutations: A case report

A novel mitochondrial DNA deletion in a patient with Kearns-Sayre syndrome: A late-onset of the fatal cardiac conduction deficit and cardiomyopathy accompanying long-term rGH treatment

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Đang chuẩn bị liên kết để tải về tài liệu: A novel mitochondrial DNA deletion in a patient with Kearns-Sayre syndrome: A late-onset of the fatal cardiac conduction deficit and cardiomyopathy accompanying long-term rGH treatment

B355252, a novel small molecule, confers neuroprotection against cobalt chloride toxicity in mouse hippocampal cells through altering mitochondrial dynamics and limiting autophagy induction

Severe clinical manifestation of mitochondrial 3-hydroxy-3-methylglutarylCoA synthase deficiency associated with two novel mutations: A case report

A novel mitochondrial DNA deletion in a patient with Kearns-Sayre syndrome: A late-onset of the fatal cardiac conduction deficit and cardiomyopathy accompanying long-term rGH treatment

The mitochondrial genome of Faughnia haani (Stomatopoda): Novel organization of the control region and phylogenetic position of the superfamily Parasquilloidea

Molecular characterization and application of a novel cytoplasmic male sterility-associated mitochondrial sequence in rice

Báo cáo khoa học: Cloning and characterization of AtNUDT13, a novel mitochondrial Arabidopsis thaliana Nudix hydrolase speciﬁc for long-chain diadenosine polyphosphates

Effects of novel pyrrolomycin MP1 in MYCN amplified chemoresistant neuroblastoma cell lines alone and combined with temsirolimus

P53R2 as a novel prognostic biomarker in nasopharyngeal carcinoma

BPIQ, a novel synthetic quinoline derivative, inhibits growth and induces mitochondrial apoptosis of lung cancer cells in vitro and in zebrafish xenograft model

Assembly and analysis of a male sterile rubber tree mitochondrial genome reveals DNA rearrangement events and a novel transcript

Đang chuẩn bị liên kết để tải về tài liệu:
A novel mitochondrial DNA deletion in a patient with Kearns-Sayre syndrome: A late-onset of the fatal cardiac conduction deficit and cardiomyopathy accompanying long-term rGH treatment