A homozygous mutation in the SCO2 gene causes a spinal muscular atrophy like presentation with stridor and respiratory insufficiency

scientific article published on 29 October 2009

A homozygous mutation in the SCO2 gene causes a spinal muscular atrophy like presentation with stridor and respiratory insufficiency is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1016/J.EJPN.2009.09.008
P698PubMed publication ID19879173

P50authorMaciej PronickiQ57420546
Dorota Piekutowska-AbramczukQ58241782
Magdalena PajdowskaQ59679776
Pawel KowalskiQ59707203
Agnieszka Karkucinska-WieckowskaQ59708179
Marek MigdalQ61861398
Jolanta Sykut-CegielskaQ62568372
Ewa PopowskaQ114529439
P2093author name stringJoanna Taybert
Elzbieta Karczmarewicz
Tamara Szymanska-Debinska
Bogumila Milewska-Bobula
P433issue3
P921main subjectspinal muscular atrophyQ580290
muscular atrophyQ2844600
homozygosityQ114049690
P304page(s)253-260
P577publication date2009-10-29
P1433published inEuropean Journal of Paediatric NeurologyQ15755269
P1476titleA homozygous mutation in the SCO2 gene causes a spinal muscular atrophy like presentation with stridor and respiratory insufficiency
P478volume14

Reverse relations

cites work (P2860)
Q37635154Affection of the Respiratory Muscles in Combined Complex I and IV Deficiency.
Q41859118Analysis of reported SCO2 gene mutations affecting cytochrome c oxidase activity in various diseases
Q38942904Copper transporters and chaperones: Their function on angiogenesis and cellular signalling
Q40259007Exome sequencing reveals SCO2 mutations in a family presented with fatal infantile hyperthermia
Q57175222Human diseases associated with defects in assembly of OXPHOS complexes
Q37094802Impaired Muscle Mitochondrial Biogenesis and Myogenesis in Spinal Muscular Atrophy.
Q37302261Left ventricular noncompaction (LVNC) and low mitochondrial membrane potential are specific for Barth syndrome.
Q30588636Mitochondrial cardioencephalomyopathy due to a novel SCO2 mutation in a Brazilian patient: case report and literature review
Q24339538Mutations in SCO2 are associated with autosomal-dominant high-grade myopia
Q36894743No Evidence for Association of SCO2 Heterozygosity with High-Grade Myopia or Other Diseases with Possible Mitochondrial Dysfunction
Q47851457SCO2 mutations cause early-onset axonal Charcot-Marie-Tooth disease associated with cellular copper deficiency

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