Human Genome Epidemiology Literature Finder
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Records 1 - 4 (of 4 Records) |
| Query Trace: Disease and PMVK[original query] |
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| Mutations in mevalonate pathway genes in patients with familial or sporadic porokeratosis. The Journal of dermatology 2018 May . Leng Yunji, Yan Lulu, Feng Hongquan, Chen Chen, Wang Shusen, Luo Yang, Cao Lih |
| Genetic risk of Parkinson disease and progression:: An analysis of 13 longitudinal cohorts. Neurology. Genetics 2019 Aug 5 (4): e348. Iwaki Hirotaka, Blauwendraat Cornelis, Leonard Hampton L, Liu Ganqiang, Maple-Grødem Jodi, Corvol Jean-Christophe, Pihlstrøm Lasse, van Nimwegen Marlies, Hutten Samantha J, Nguyen Khanh-Dung H, Rick Jacqueline, Eberly Shirley, Faghri Faraz, Auinger Peggy, Scott Kirsten M, Wijeyekoon Ruwani, Van Deerlin Vivianna M, Hernandez Dena G, Day-Williams Aaron G, Brice Alexis, Alves Guido, Noyce Alastair J, Tysnes Ole-Bjørn, Evans Jonathan R, Breen David P, Estrada Karol, Wegel Claire E, Danjou Fabrice, Simon David K, Ravina Bernard, Toft Mathias, Heutink Peter, Bloem Bastiaan R, Weintraub Daniel, Barker Roger A, Williams-Gray Caroline H, van de Warrenburg Bart P, Van Hilten Jacobus J, Scherzer Clemens R, Singleton Andrew B, Nalls Mike |
| Inflammatory linear verrucous epidermal nevus (ILVEN) encompasses a spectrum of inflammatory mosaic disorders. Pediatric dermatology 2022 7 39 (6): 903-907. Atzmony Lihi, Ugwu Nelson, Hamilton Claire, Paller Amy S, Zech Loren, Antaya Richard J, Choate Keith |
| A novel PMVK variant associated with familial porokeratosis. Human heredity 2023 6 . Wenjing Zhang, Xinmiao Nie, Lei Shi, Fengmin Shao, Lihua C |
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