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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 3 (of 3 Records)

Query Trace: Hearing Loss and PMP22[original query]
Modifier Gene Candidates in Charcot-Marie-Tooth Disease Type 1A: A Case-Only Genome-Wide Association Study. GWAS Catalog
Journal of neuromuscular diseases 2019 6 (2): 201-211.
Tao Feifei, Beecham Gary W, Rebelo Adriana P, Blanton Susan H, Moran John J, Lopez-Anido Camila, Svaren John, Abreu Lisa, Rizzo Devon, Kirk Callyn A, Wu Xingyao, Feely Shawna, Verhamme Camiel, Saporta Mario A, Herrmann David N, Day John W, Sumner Charlotte J, Lloyd Thomas E, Li Jun, Yum Sabrina W, Taroni Franco, Baas Frank, Choi Byung-Ok, Pareyson Davide, Scherer Steven S, Reilly Mary M, Shy Michael E, Züchner Stephan,
PMP22 Gene-Associated Neuropathies: Phenotypic Spectrum in a Cohort from India.
Journal of molecular neuroscience : MN 2020 1 70 (5): 778-789.
Nagappa Madhu, Sharma Shivani, Govindaraj Periyasamy, Chickabasaviah Yasha T, Siram Ramesh, Shroti Akhilesh, Debnath Monojit, Sinha Sanjib, Bindu Parayil S, Taly Arun
Charcot-Marie-Tooth disease misdiagnosed as chronic inflammatory demyelinating polyradiculoneuropathy: An international multicentric retrospective study.
European journal of neurology 2021 6 28 (9): 2846-2854.
Hauw Fabien, Fargeot Guillaume, Adams David, Attarian Shahram, Cauquil Cécile, Chanson Jean-Baptiste, Créange Alain, Gendre Thierry, Deiva Kumaran, Delmont Emilien, Francou Bruno, Genestet Steeve, Kuntzer Thierry, Latour Philippe, Le Masson Gwendal, Magy Laurent, Nardin Clotilde, Ochsner François, Sole Guilhem, Stojkovic Tanya, Maisonobe Thierry, Tard Céline, Van den Berghe Peter, Echaniz-Laguna Ando
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