HuGE Literature Finder
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| Phenotypic expression and clinical outcomes in a South Asian PRKAG2 cardiomyopathy cohort. Scientific reports 2020 11 10 (1): 20610. Ahamed Hisham, Balegadde Aniketh Vijay, Menon Shilpa, Menon Ramesh, Ramachandran Aishwarya, Mathew Navin, Natarajan K U, Nair Indu Ramachandran, Kannan Rajesh, Shankar Meghna, Mathew Oommen K, Nguyen Thong T, Gupta Ravi, Stawiski Eric W, Ramprasad V L, Seshagiri Somasekar, Phalke Same |
| Wolff-Parkinson-White syndrome: De novo variants and evidence for mutational burden in genes associated with atrial fibrillation. American journal of medical genetics. Part A 2020 4 182 (6): 1387-1399. Coban-Akdemir Zeynep H, Charng Wu-Lin, Azamian Mahshid, Paine Ingrid S, Punetha Jaya, Grochowski Christopher M, Gambin Tomasz, Valdes Santiago O, Cannon Bryan, Zapata Gladys, Hernandez Patricia P, Jhangiani Shalini, Doddapaneni Harsha, Hu Jianhong, Boricha Fatima, Muzny Donna M, Boerwinkle Eric, Yang Yaping, Gibbs Richard A, Posey Jennifer E, Wehrens Xander H T, Belmont John W, Kim Jeffrey J, Miyake Christina Y, Lupski James R, Lalani Seema |
| Patient with a PRKAG2 mutation who developed Immunoglobulin A nephropathy: a case report. European heart journal. Case reports 2019 8 3 (2): . Giudici Michael C, Ahmad Ferhaan, Holanda Danniele |
| Sarcomere protein gene mutations in patients with apical hypertrophic cardiomyopathy. Circulation. Cardiovascular genetics 2011 Jun 4 (3): 288-95. Gruner Christiane, Care Melanie, Siminovitch Katherine, Moravsky Gil, Wigle E Douglas, Woo Anna, Rakowski Har |
| Shared genetic causes of cardiac hypertrophy in children and adults. The New England journal of medicine 2008 May 358 (18): 1899-908. Morita Hiroyuki, Rehm Heidi L, Menesses Andres, McDonough Barbara, Roberts Amy E, Kucherlapati Raju, Towbin Jeffrey A, Seidman J G, Seidman Christine |
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