Recurrent myoglobinuria due to carnitine palmitoyltransferase II deficiency: clinical, biochemical, and genetic features of adult-onset cases. (Q36073843)

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English	Recurrent myoglobinuria due to carnitine palmitoyltransferase II deficiency: clinical, biochemical, and genetic features of adult-onset cases.	scientific article

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scholarly article

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15776096%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

Recurrent myoglobinuria due to carnitine palmitoyltransferase II deficiency: clinical, biochemical, and genetic features of adult-onset cases (English)

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15776096%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

carnitine palmitoyltransferase II deficiency

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Peter George

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Europe PubMed Central

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9 January 2020

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Dean Kilfoyle

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9 January 2020

David Hutchinson

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9 January 2020

Howard Potter

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9 January 2020

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25 February 2005

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9 January 2020

The New Zealand Medical Journal

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9 January 2020

118

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9 January 2020

1210

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9 January 2020

U1320

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9 January 2020

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9 January 2020

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