(Q48131655)

English

Multiple cerebral cavernous malformations and a novel CCM3 germline deletion in a German family.

scientific article published on 11 July 2010

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scholarly article

1 reference

Europe PubMed Central

8 February 2018

http://europepmc.org/abstract/MED/20623299

Multiple cerebral cavernous malformations and a novel CCM3 germline deletion in a German family. (English)

1 reference

Europe PubMed Central

8 February 2018

http://europepmc.org/abstract/MED/20623299

Elisabeth Tournier-Lasserve

4

1 reference

Europe PubMed Central

8 February 2018

http://europepmc.org/abstract/MED/20623299

5

object named as

Michael Orth

1 reference

Europe PubMed Central

8 February 2018

http://europepmc.org/abstract/MED/20623299

author name string

Chi-un Choe

1

1 reference

Europe PubMed Central

8 February 2018

http://europepmc.org/abstract/MED/20623299

Florence Riant

2

1 reference

Europe PubMed Central

8 February 2018

http://europepmc.org/abstract/MED/20623299

Christian Gerloff

3

1 reference

Europe PubMed Central

8 February 2018

http://europepmc.org/abstract/MED/20623299

publication date

11 July 2010

1 reference

Europe PubMed Central

8 February 2018

http://europepmc.org/abstract/MED/20623299

Journal of Neurology

1 reference

Europe PubMed Central

8 February 2018

http://europepmc.org/abstract/MED/20623299

257

1 reference

Europe PubMed Central

8 February 2018

http://europepmc.org/abstract/MED/20623299

12

1 reference

Europe PubMed Central

8 February 2018

http://europepmc.org/abstract/MED/20623299

2097-2098

1 reference

Europe PubMed Central

8 February 2018

http://europepmc.org/abstract/MED/20623299

https://scigraph.springernature.com/pub.10.1007/s00415-010-5648-7

0 references

Multilocus linkage identifies two new loci for a mendelian form of stroke, cerebral cavernous malformation, at 7p15-13 and 3q25.2-27.

1 reference

https://pubmed.ncbi.nlm.nih.gov/20623299

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetics of cavernous angiomas

1 reference

https://pubmed.ncbi.nlm.nih.gov/20623299

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

CCM3 mutations are uncommon in cerebral cavernous malformations

1 reference

https://pubmed.ncbi.nlm.nih.gov/20623299

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Different spectra of genomic deletions within the CCM genes between Italian and American CCM patient cohorts

1 reference

https://pubmed.ncbi.nlm.nih.gov/20623299

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Low frequency of PDCD10 mutations in a panel of CCM3 probands: potential for a fourth CCM locus

1 reference

https://pubmed.ncbi.nlm.nih.gov/20623299

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in apoptosis-related gene, PDCD10, cause cerebral cavernous malformation 3.

1 reference

https://pubmed.ncbi.nlm.nih.gov/20623299

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00415-010-5648-7

1 reference

Europe PubMed Central

8 February 2018

http://europepmc.org/abstract/MED/20623299

1 reference

Europe PubMed Central

8 February 2018

http://europepmc.org/abstract/MED/20623299

ResearchGate publication ID

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