Difference between revisions of "SMARCA4"

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(+sinonasal)
Line 3: Line 3:
*[[SMARCA4-deficient pulmonary adenocarcinoma]].
*[[SMARCA4-deficient pulmonary adenocarcinoma]].
*[[Ovarian small cell carcinoma of the hypercalcemic type]].
*[[Ovarian small cell carcinoma of the hypercalcemic type]].
*SMARCA4-deficient sinonasal carcinoma.<ref>{{cite journal |authors=Kakkar A, Ashraf SF, Rathor A, Adhya AK, Mani S, Sikka K, Jain D |title=SMARCA4/BRG1-Deficient Sinonasal Carcinoma |journal=Arch Pathol Lab Med |volume=146 |issue=9 |pages=1122–1130 |date=September 2022 |pmid=34871352 |doi=10.5858/arpa.2021-0001-OA |url=}}</ref>


==References==
==References==

Revision as of 14:16, 6 October 2023

SMARCA4, also BRG1,[1] is a gene mutated in:

References

  1. Online 'Mendelian Inheritance in Man' (OMIM) 603254
  2. Kakkar A, Ashraf SF, Rathor A, Adhya AK, Mani S, Sikka K, Jain D (September 2022). "SMARCA4/BRG1-Deficient Sinonasal Carcinoma". Arch Pathol Lab Med 146 (9): 1122–1130. doi:10.5858/arpa.2021-0001-OA. PMID 34871352.