Expanding the clinical phenotype of FADD deficiency with a novel mutation and its role in Fas‐mediated apoptotic pathway.

Autor:	Setia, Priyanka, Bargir, Umair Ahmed, Shanmukhaiah, Chandrakala, Jodhawat, Neha, Gaikwad, Pallavi, Vedpathak, Disha, Dutta, Shubhankar, Kulkarni, Rucha, Kambli, Priyanka, Dalvi, Aparna, Shinde, Shweta, Gupta, Maya, Nambiar, Nayana, Sawant, Sneha, Shelar, Shraddha, Dhawale, Amruta, Mohanty, Madhu, Yadav, Reetika Malik, Bose, Kakoli, Madkaikar, Manisha
Předmět:	LYMPHADENITIS HUMAN cytomegalovirus diseases GENETIC mutation PHENOTYPES DEATH receptors AUTOIMMUNE diseases INFORMED consent (Medical law)
Zdroj:	British Journal of Haematology; Jul2023, Vol. 202 Issue 2, pe11-e15, 5p
Databáze:	Complementary Index
Externí odkaz:	Zobrazit plný text záznamu Plný text