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gne in Homo sapiensMus musculusRattus norvegicusAll 594 Gene records
GeneReviews® [Internet].
Adam MP, Feldman J, Mirzaa GM, et al., editors.
Seattle (WA): University of Washington, Seattle; 1993-2024.
GeneReviews by Title GeneReviews Advanced Search Help
GNE Myopathy.
Carrillo N, Malicdan MC, Huizing M. 2004 Mar 26 [Updated 2020 Apr 9].
MYH9-Related Disease.
Savoia A, Pecci A. 2008 Nov 20 [Updated 2021 Feb 18].
Resources for Genetics Professionals — Genetic Disorders Associated with Founder Variants Common in the Romani Population.
Wallace SE. 2022 Aug 11.
Dysferlinopathy.
Aoki M, Takahashi T. 2004 Feb 5 [Updated 2021 May 27].
Myotonic Dystrophy Type 2.
Schoser B. 2006 Sep 21 [Updated 2020 Mar 19].
Alpha-Mannosidosis.
Malm D, Nilssen Ø. 2001 Oct 11 [Updated 2019 Jul 18].
Laing Distal Myopathy.
Lamont P, Laing NG. 2006 Oct 17 [Updated 2021 Feb 4].
Udd Distal Myopathy – Tibial Muscular Dystrophy.
Udd B, Hackman P. 2005 Feb 17 [Updated 2020 Jan 2].
Charcot-Marie-Tooth Hereditary Neuropathy Overview.
Bird TD. 1998 Sep 28 [Updated 2023 Mar 14].
ANO5 Muscle Disease.
Penttilä S, Vihola A, Palmio J, et al. 2012 Nov 29 [Updated 2019 Aug 22].
Resources for Genetics Professionals — Genetic Disorders Associated with Founder Variants Common in the Sephardic Jewish Population.
Wallace SE, Mirzaa GM. 2023 Jan 12.
Facioscapulohumeral Muscular Dystrophy.
Preston MK, Tawil R, Wang LH. 1999 Mar 8 [Updated 2020 Feb 6].
Inclusion Body Myopathy with Paget Disease of Bone and/or Frontotemporal Dementia.
Kimonis V. 2007 May 25 [Updated 2019 Sep 12].
Myotonic Dystrophy Type 1.
Bird TD. 1999 Sep 17 [Updated 2021 Mar 25].
Free Sialic Acid Storage Disorders.
Adams D, Wasserstein M. 2003 Jun 13 [Updated 2020 Jan 23].
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