Homo sapiens GDAP1 mRNA for truncated ganglioside differentiation asso - Nucleotide

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Genetic and clinical profile of 15 Chinese families with GDAP1-related Charcot-Marie-Tooth disease and identification of H256R as a frequent mutation. [J Peripher Nerv Syst. 2024]
Genetic and clinical profile of 15 Chinese families with GDAP1-related Charcot-Marie-Tooth disease and identification of H256R as a frequent mutation.
Li Z, Zeng S, Xie Y, Li X, Huang S, Zhao H, Cao W, Liu L, Wang M, Gong Q, et al. J Peripher Nerv Syst. 2024 Jun; 29(2):232-242. Epub 2024 May 5.
Antagonistic roles of canonical and Alternative-RPA in disease-associated tandem CAG repeat instability. [Cell. 2023]
Antagonistic roles of canonical and Alternative-RPA in disease-associated tandem CAG repeat instability.
Gall-Duncan T, Luo J, Jurkovic CM, Fischer LA, Fujita K, Deshmukh AL, Harding RJ, Tran S, Mehkary M, Li V, et al. Cell. 2023 Oct 26; 186(22):4898-4919.e25. Epub 2023 Oct 11.
Homozygous Mutations in GDAP1 and MFN2 Genes Resulted in Autosomal Recessive Forms of Charcot-Marie-Tooth Disease in Consanguineous Pakistani Families. [DNA Cell Biol. 2023]
Homozygous Mutations in GDAP1 and MFN2 Genes Resulted in Autosomal Recessive Forms of Charcot-Marie-Tooth Disease in Consanguineous Pakistani Families.
Asif M, Chiou CC, Hussain MF, Hussain M, Sajid Z, Gulsher M, Raheem A, Khan A, Nasreen N, Kloczkowski A, et al. DNA Cell Biol. 2023 Nov; 42(11):697-708. Epub 2023 Oct 5.

RefSeq alternative splicing
See 10 reference mRNA sequence splice variants for the GDAP1 gene.

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Nucleotide