A91V is a polymorphism in the perforin gene not causative of an FHLH phenotype.
Publication
, Journal Article
Zur Stadt, U; Beutel, K; Weber, B; Kabisch, H; Schneppenheim, R; Janka, G
Published in: Blood
September 15, 2004
Duke Scholars
Published In
Blood
DOI
ISSN
0006-4971
Publication Date
September 15, 2004
Volume
104
Issue
6
Start / End Page
1909
Location
United States
Related Subject Headings
- Valine
- Pore Forming Cytotoxic Proteins
- Polymorphism, Genetic
- Phenotype
- Perforin
- Mutation, Missense
- Membrane Glycoproteins
- Immunology
- Humans
- Histiocytosis, Non-Langerhans-Cell
Citation
APA
Chicago
ICMJE
MLA
NLM
Zur Stadt, U., Beutel, K., Weber, B., Kabisch, H., Schneppenheim, R., & Janka, G. (2004). A91V is a polymorphism in the perforin gene not causative of an FHLH phenotype. Blood, 104(6), 1909. https://doi.org/10.1182/blood-2004-02-0733
Zur Stadt, Udo, Karin Beutel, Belinda Weber, Hartmut Kabisch, Reinhard Schneppenheim, and Gritta Janka. “A91V is a polymorphism in the perforin gene not causative of an FHLH phenotype.” Blood 104, no. 6 (September 15, 2004): 1909. https://doi.org/10.1182/blood-2004-02-0733.
Zur Stadt U, Beutel K, Weber B, Kabisch H, Schneppenheim R, Janka G. A91V is a polymorphism in the perforin gene not causative of an FHLH phenotype. Blood. 2004 Sep 15;104(6):1909.
Zur Stadt, Udo, et al. “A91V is a polymorphism in the perforin gene not causative of an FHLH phenotype.” Blood, vol. 104, no. 6, Sept. 2004, p. 1909. Pubmed, doi:10.1182/blood-2004-02-0733.
Zur Stadt U, Beutel K, Weber B, Kabisch H, Schneppenheim R, Janka G. A91V is a polymorphism in the perforin gene not causative of an FHLH phenotype. Blood. 2004 Sep 15;104(6):1909.
Published In
Blood
DOI
ISSN
0006-4971
Publication Date
September 15, 2004
Volume
104
Issue
6
Start / End Page
1909
Location
United States
Related Subject Headings
- Valine
- Pore Forming Cytotoxic Proteins
- Polymorphism, Genetic
- Phenotype
- Perforin
- Mutation, Missense
- Membrane Glycoproteins
- Immunology
- Humans
- Histiocytosis, Non-Langerhans-Cell