Missing Full Disclosures

Correction for:  Noda K, Hattori Y, Hori M, Harada-Shiba M, Ihara M. A Case of Multiple Intracranial Major Artery Stenoses With Coexisting PCSK9 p.E32K and RNF213 p.R4810K Variants. Neurol Genet. 2023 Sep 5;9(5):e200099. doi: 10.1212/NXG.0000000000200099.  PMID: 38235366

Correction for: Laliberté A, Myers KA. Ataxia and Diplopia: A New SCN8A-Related Phenotype. Neurol Genet. 2023 Jul 10;9(4):e200085. doi: 10.1212/NXG.0000000000200085.  PMID: 37440794

Correction for: Xiao C, Cassini T, Benavides D, Ebrahim A, Adams D, Toro C.  Genomic Diagnoses for Ectopic Intracerebral Calcifications. Neurol Genet. 2023 Aug 2;9(5):e200083. doi: 10.1212/NXG.0000000000200083. PMID: 37547187

Correction for: Sennfält S, Aspegren O, Engvall M, Granberg T, Piehl F. Systemic Capillary Leak Syndrome With Cerebral Involvement in a C9orf72 Expansion Carrier: Case Report and Review of the Literature.Neurol Genet. 2023 Jun 14;9(4):e200081. doi: 10.1212/NXG.0000000000200081. PMID: 37334257

Correction for: Manco C, Cortese R, Alberti M, Bianchi S, Monti L, De Stefano N, Battisti C. FOLR1 Gene Variation With Adult-Onset Cerebral Folate Deficiency and Stable Clinical and MRI Features up to 2 Years. Neurol Genet. 2023 Oct 24;9(6):e200104. doi: 10.1212/NXG.0000000000200104. PMID: 38239817Correction for: Williams EK, Shea C, Gonzalez-Perez P. Agenesis of Pectoralis Major Muscle in Late-Onset GFPT1-Related Congenital Myasthenic Syndrome: A Case Report. Neurol Genet. 2023 Sep 26;9(6):e200102. doi: 10.1212/NXG.0000000000200102.  PMID: 38235042

Correction for: Langbehn DR, Sathe SS, Loy C, Sampaio C, Mccusker EA. A Phenotypic Atlas for Huntington Disease Based on Data From the Enroll-HD Cohort Study. Neurol Genet. 2023 Nov 28;9(6):e200111. doi: 10.1212/NXG.0000000000200111. PMID: 38035176Correction for: Wong KN, Botto LD, He M, Baker PR 2nd, Vanderver AL, Bonkowsky JL. Novel SLC13A3 Variants and Cases of Acute Reversible Leukoencephalopathy and α-Ketoglutarate Accumulation and Literature Review. Neurol Genet. 2023 Sep 26;9(6):e200101. doi: 10.1212/NXG.0000000000200101.  PMID: 38235040