(Q48020579)

English

Frequent de novo monoallelic expression of beta-spectrin gene (SPTB) in children with hereditary spherocytosis and isolated spectrin deficiency.

scientific article published in May 1998

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scholarly article

1 reference

Europe PubMed Central

7 February 2018

http://europepmc.org/abstract/MED/9609518

Frequent de novo monoallelic expression of beta-spectrin gene (SPTB) in children with hereditary spherocytosis and isolated spectrin deficiency. (English)

1 reference

Europe PubMed Central

7 February 2018

http://europepmc.org/abstract/MED/9609518

hereditary spherocytosis

1 reference

based on heuristic

inferred from title

author name string

Miraglia del Giudice E

1

1 reference

Europe PubMed Central

7 February 2018

http://europepmc.org/abstract/MED/9609518

Lombardi C

2

1 reference

Europe PubMed Central

7 February 2018

http://europepmc.org/abstract/MED/9609518

Francese M

3

1 reference

Europe PubMed Central

7 February 2018

http://europepmc.org/abstract/MED/9609518

Nobili B

4

1 reference

Europe PubMed Central

7 February 2018

http://europepmc.org/abstract/MED/9609518

Conte ML

5

1 reference

Europe PubMed Central

7 February 2018

http://europepmc.org/abstract/MED/9609518

Amendola G

6

1 reference

Europe PubMed Central

7 February 2018

http://europepmc.org/abstract/MED/9609518

Cutillo S

7

1 reference

Europe PubMed Central

7 February 2018

http://europepmc.org/abstract/MED/9609518

Iolascon A

8

1 reference

Europe PubMed Central

7 February 2018

http://europepmc.org/abstract/MED/9609518

Perrotta S

9

1 reference

Europe PubMed Central

7 February 2018

http://europepmc.org/abstract/MED/9609518

language of work or name

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publication date

1 May 1998

1 reference

Europe PubMed Central

7 February 2018

http://europepmc.org/abstract/MED/9609518

British Journal of Haematology

1 reference

Europe PubMed Central

7 February 2018

http://europepmc.org/abstract/MED/9609518

101

1 reference

Europe PubMed Central

7 February 2018

http://europepmc.org/abstract/MED/9609518

251-254

1 reference

Europe PubMed Central

7 February 2018

http://europepmc.org/abstract/MED/9609518

2

1 reference

Europe PubMed Central

7 February 2018

http://europepmc.org/abstract/MED/9609518

Beta spectrin kissimmee: a spectrin variant associated with autosomal dominant hereditary spherocytosis and defective binding to protein 4.1.

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2141.1998.00688.X

21 January 2018

Human gene mutations affecting RNA processing and translation

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2141.1998.00688.X

21 January 2018

Molecular basis of spectrin deficiency in beta spectrin Durham. A deletion within beta spectrin adjacent to the ankyrin-binding site precludes spectrin attachment to the membrane in hereditary spherocytosis

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2141.1998.00688.X

21 January 2018

Combination of two mutant alpha spectrin alleles underlies a severe spherocytic hemolytic anemia

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2141.1998.00688.X

21 January 2018

Identifiers

10.1046/J.1365-2141.1998.00688.X

1 reference

Europe PubMed Central

7 February 2018

http://europepmc.org/abstract/MED/9609518

1 reference

Europe PubMed Central

7 February 2018

http://europepmc.org/abstract/MED/9609518

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