(Q40271117)

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A novel activating mutation in transmembrane helix 6 of the thyrotropin receptor as cause of hereditary nonautoimmune hyperthyroidism.

scientific article published on May 2006

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Europe PubMed Central

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16756474

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16756474%20AND%20SRC:MED&resulttype=core&format=json

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29 January 2020

title

A novel activating mutation in transmembrane helix 6 of the thyrotropin receptor as cause of hereditary nonautoimmune hyperthyroidism (English)

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16756474

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16756474%20AND%20SRC:MED&resulttype=core&format=json

retrieved

29 January 2020

main subject

transmembrane protein

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author

Benjamin U Nwosu

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1

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Europe PubMed Central

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16756474

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16756474%20AND%20SRC:MED&resulttype=core&format=json

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29 January 2020

author name string

Loukas Gourgiotis

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2

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Europe PubMed Central

PubMed publication ID

16756474

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16756474%20AND%20SRC:MED&resulttype=core&format=json

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29 January 2020

Marvin C Gershengorn

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3

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16756474

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16756474%20AND%20SRC:MED&resulttype=core&format=json

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29 January 2020

Susanne Neumann

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4

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16756474

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29 January 2020

publication date

1 May 2006

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16756474

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16756474%20AND%20SRC:MED&resulttype=core&format=json

29 January 2020

1 reference

Europe PubMed Central

PubMed publication ID

16756474

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16756474%20AND%20SRC:MED&resulttype=core&format=json

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29 January 2020

volume

16

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16756474

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29 January 2020

issue

5

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16756474

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29 January 2020

page(s)

505-512

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PubMed publication ID

16756474

reference URL

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(Q40271117)

A novel activating mutation in transmembrane helix 6 of the thyrotropin receptor as cause of hereditary nonautoimmune hyperthyroidism.

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