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Identification and characterization of human GDF15 knockouts.
Gurtan AM, Khalid S, Koch C, Khan MZ, Lamarche LB, Splawski I, Dolan E, Carrion AM, Zessis R, Clement ME, Chen Z, Lindsley LD, Chiu YH, Streeper RS, Denning DP, Goldfine AB, Doyon B, Abbasi A, Harrow JL, Tsunoyama K, Asaumi M, Kou I, Shuldiner AR, Rodriguez-Flores JL, Rasheed A, Jahanzaib M, Mian MR, Liaqat MB, Raza SS, Sultana R, Jalal A, Saeed MH, Abbas S, Memon FR, Ishaq M, Dominy JE, Saleheen D. Gurtan AM, et al. Among authors: khan mz. Nat Metab. 2024 Sep 26. doi: 10.1038/s42255-024-01135-3. Online ahead of print. Nat Metab. 2024. PMID: 39327531
Pathogenic SATB2 missense variants affecting p.Gly392 have variable functional implications and result in diverse clinical phenotypes.
den Hoed J, Hashimoto H, Khan M, Semmekrot F, Bosanko KA, Abe-Hatano C, Nakagawa E, Venselaar H, Quercia N, Chad L, Kurosaka H, Rondeau S, Fisher SE, Yamamoto S, Zarate YA. den Hoed J, et al. Among authors: khan m. J Med Genet. 2024 Sep 26:jmg-2024-110015. doi: 10.1136/jmg-2024-110015. Online ahead of print. J Med Genet. 2024. PMID: 39327041
The Surgical Significance of Phenotypic Variability in the Setting of Tetralogy of Fallot.
Chowdhury UK, Anderson RH, Spicer DE, Pandey NN, Gupta SK, George N, Khan MA, Chittimuri C. Chowdhury UK, et al. Among authors: khan ma. World J Pediatr Congenit Heart Surg. 2024 Sep 26:21501351241274731. doi: 10.1177/21501351241274731. Online ahead of print. World J Pediatr Congenit Heart Surg. 2024. PMID: 39324176 Review.
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