Human Genome Epidemiology Literature Finder
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Records 1 - 3 (of 3 Records) |
| Query Trace: Disease and UFM1[original query] |
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Genome-wide association studies identify genetic loci for low von Willebrand factor levels.
European journal of human genetics : EJHG 2015 Oct . van Loon Janine, Dehghan Abbas, Weihong Tang, Trompet Stella, McArdle Wendy L, Asselbergs Folkert F W, Chen Ming-Huei, Lopez Lorna M, Huffman Jennifer E, Leebeek Frank W G, Basu Saonli, Stott David J, Rumley Ann, Gansevoort Ron T, Davies Gail, Wilson James J F, Witteman Jacqueline C M, Cao Xiting, de Craen Anton J M, Bakker Stephan J L, Psaty Bruce M, Starr John M, Hofman Albert, Wouter Jukema J, Deary Ian J, Hayward Caroline, van der Harst Pim, Lowe Gordon D O, Folsom Aaron R, Strachan David P, Smith Nicolas, de Maat Moniek P M, O'Donnell Christoph |
| UFM1 founder mutation in the Roma population causes recessive variant of H-ABC. Neurology 2017 Sep . Hamilton Eline M C, Bertini Enrico, Kalaydjieva Luba, Morar Bharti, Doj?áková Dana, Liu Judy, Vanderver Adeline, Curiel Julian, Persoon Claudia M, Diodato Daria, Pinelli Lorenzo, van der Meij Nathalie L, Plecko Barbara, Blaser Susan, Wolf Nicole I, Waisfisz Quinten, Abbink Truus E M, van der Knaap Marjo S, |
| Neuroimaging to Genotype: Delineating the Spectrum of Disorders With Deficient Myelination in the Indian Population. American journal of medical genetics. Part A 2024 10 e63914. Namanpreet Kaur, Michelle C do Rosario, Purvi Majethia, Selinda Mascarenhas, Lakshmi Priya Rao, Karthik Vijay Nair, Bhagesh Hunakunti, Adarsh Pooradan Prasannakumar, Rohit Naik, Dhanya Lakshmi Narayanan, Shalini S Nayak, Vivekananda Bhat, Suvasini Sharma, Y Ramesh Bhat, B L Yatheesha, Rajesh Kulkarni, Siddaramappa J Patil, Sheela Nampoothiri, Shahyan Siddiqui, Katta Mohan Girisha, Stephanie Bielas, Anju Shuk |
- Page last reviewed:Feb 1, 2024
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