Development, characterization, and hematopoietic differentiation of Griscelli syndrome type 2 induced pluripotent stem cells

BACKGROUND: Griscelli syndrome type 2 (GS-2) is a rare, autosomal recessive immune deficiency syndrome caused by a mutation in the RAB27A gene, which results in the absence of a protein involved in vesicle trafficking and consequent loss of function of in particular cytotoxic T and NK cells. Induced...

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Detalles Bibliográficos
Autores principales: Güney-Esken, Gülen, Erol, Özgür Doğuş, Pervin, Burcu, Gürhan Sevinç, Gülben, Önder, Tamer, Bilgiç, Elif, Korkusuz, Petek, Günel-Özcan, Ayşen, Uçkan-Çetinkaya, Duygu, Aerts-Kaya, Fatima
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8117610/
https://www.ncbi.nlm.nih.gov/pubmed/33985578
http://dx.doi.org/10.1186/s13287-021-02364-z

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8117610/
https://www.ncbi.nlm.nih.gov/pubmed/33985578
http://dx.doi.org/10.1186/s13287-021-02364-z

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