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POLG mutations associated with Alpers' syndrome and mitochondrial DNA depletion

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15122711

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POLG mutations associated with Alpers' syndrome and mitochondrial DNA depletion (English)

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Robert K Naviaux

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Khue V Nguyen

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1 May 2004

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Annals of Neurology

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55

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5

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706-712

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cites work

Infantile Diffuse Cerebral Degeneration With Hepatic Cirrhosis

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https://api.crossref.org/works/10.1002%2FANA.20079

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21 January 2018

Mitochondrial DNA depletion: mutations in thymidine kinase gene with myopathy and SMA.

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https://api.crossref.org/works/10.1002%2FANA.20079

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21 January 2018

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10.1002/ANA.20079

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15122711

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20 December 2017

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http://europepmc.org/abstract/MED/15122711

PubMed publication ID

15122711

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Europe PubMed Central

PubMed publication ID

15122711

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20 December 2017

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(Q46178330)

POLG mutations associated with Alpers' syndrome and mitochondrial DNA depletion

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