(Q51937484)

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Infantile-onset glycogen storage disease type II (Pompe disease): report of a case with genetic diagnosis and pathological findings.

scientific article published in May 2004

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Europe PubMed Central

PubMed publication ID

15366815

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15366815%20AND%20SRC:MED&resulttype=core&format=json

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title

Infantile-onset glycogen storage disease type II (Pompe disease): report of a case with genetic diagnosis and pathological findings (English)

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Europe PubMed Central

PubMed publication ID

15366815

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15366815%20AND%20SRC:MED&resulttype=core&format=json

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1 January 2020

main subject

glycogen storage disease

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Yao-Tun Teng

1

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Europe PubMed Central

PubMed publication ID

15366815

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15366815%20AND%20SRC:MED&resulttype=core&format=json

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1 January 2020

Wen-Jen Su

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2

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Europe PubMed Central

PubMed publication ID

15366815

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1 January 2020

Jia-Wei Hou

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3

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PubMed publication ID

15366815

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Shiu-Feng Huang

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4

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15366815

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1 January 2020

publication date

1 May 2004

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PubMed publication ID

15366815

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1 January 2020

published in

Chang Gung medical journal

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PubMed publication ID

15366815

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1 January 2020

volume

27

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PubMed publication ID

15366815

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issue

5

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15366815

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1 January 2020

page(s)

379-384

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PubMed publication ID

15366815

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1 January 2020

Identifiers

PubMed publication ID

15366815

1 reference

stated in

Europe PubMed Central

PubMed publication ID

15366815

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15366815%20AND%20SRC:MED&resulttype=core&format=json

(Q51937484)

Infantile-onset glycogen storage disease type II (Pompe disease): report of a case with genetic diagnosis and pathological findings.

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