(Q37674824)

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Genotype-phenotype correlations in laminopathies: how does fate translate?

scientific article published on February 2010

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Europe PubMed Central

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20074070

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20074070%20AND%20SRC:MED&resulttype=core&format=json

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16 January 2020

review article

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Europe PubMed Central

title

Genotype-phenotype correlations in laminopathies: how does fate translate? (English)

1 reference

stated in

Europe PubMed Central

PubMed ID

20074070

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20074070%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

1 reference

1

1 reference

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Europe PubMed Central

PubMed ID

20074070

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20074070%20AND%20SRC:MED&resulttype=core&format=json

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16 January 2020

Peter S Zammit

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4

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Europe PubMed Central

PubMed ID

20074070

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20074070%20AND%20SRC:MED&resulttype=core&format=json

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16 January 2020

author name string

Viola F Gnocchi

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2

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PubMed ID

20074070

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20074070%20AND%20SRC:MED&resulttype=core&format=json

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16 January 2020

Juliet A Ellis

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3

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PubMed ID

20074070

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20074070%20AND%20SRC:MED&resulttype=core&format=json

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publication date

1 February 2010

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20074070

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16 January 2020

published in

Biochemical Society Transactions

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Europe PubMed Central

PubMed ID

20074070

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20074070%20AND%20SRC:MED&resulttype=core&format=json

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16 January 2020

volume

38

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PubMed ID

20074070

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16 January 2020

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Pt 1

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PubMed ID

20074070

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16 January 2020

page(s)

257-262

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Europe PubMed Central

PubMed ID

20074070

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16 January 2020

cites work

Defects in cell spreading and ERK1/2 activation in fibroblasts with lamin A/C mutations

1 reference

1 April 2022

https://opencitations.net/index/coci/api/v1/citations/10.1016/J.BBADIS.2009.05.007

Recurrent de novo point mutations in lamin A cause Hutchinson–Gilford progeria syndrome

(Q37674824)

Genotype-phenotype correlations in laminopathies: how does fate translate?

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