These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
7. Utility of whole exome sequencing for the early diagnosis of pediatric-onset cerebellar atrophy associated with developmental delay in an inbred population. Megahed H; Nicouleau M; Barcia G; Medina-Cano D; Siquier-Pernet K; Bole-Feysot C; Parisot M; Masson C; Nitschké P; Rio M; Bahi-Buisson N; Desguerre I; Munnich A; Boddaert N; Colleaux L; Cantagrel V Orphanet J Rare Dis; 2016 May; 11(1):57. PubMed ID: 27146152 [TBL] [Abstract][Full Text] [Related]
8. Recurrent De Novo and Biallelic Variation of ATAD3A, Encoding a Mitochondrial Membrane Protein, Results in Distinct Neurological Syndromes. Harel T; Yoon WH; Garone C; Gu S; Coban-Akdemir Z; Eldomery MK; Posey JE; Jhangiani SN; Rosenfeld JA; Cho MT; Fox S; Withers M; Brooks SM; Chiang T; Duraine L; Erdin S; Yuan B; Shao Y; Moussallem E; Lamperti C; Donati MA; Smith JD; McLaughlin HM; Eng CM; Walkiewicz M; Xia F; Pippucci T; Magini P; Seri M; Zeviani M; Hirano M; Hunter JV; Srour M; Zanigni S; Lewis RA; Muzny DM; Lotze TE; Boerwinkle E; ; ; Gibbs RA; Hickey SE; Graham BH; Yang Y; Buhas D; Martin DM; Potocki L; Graziano C; Bellen HJ; Lupski JR Am J Hum Genet; 2016 Oct; 99(4):831-845. PubMed ID: 27640307 [TBL] [Abstract][Full Text] [Related]
9. A novel splice variant in EMC1 is associated with cerebellar atrophy, visual impairment, psychomotor retardation with epilepsy. Geetha TS; Lingappa L; Jain AR; Govindan H; Mandloi N; Murugan S; Gupta R; Vedam R Mol Genet Genomic Med; 2018 Mar; 6(2):282-287. PubMed ID: 29271071 [TBL] [Abstract][Full Text] [Related]
10. EMC10 homozygous variant identified in a family with global developmental delay, mild intellectual disability, and speech delay. Umair M; Ballow M; Asiri A; Alyafee Y; Al Tuwaijri A; Alhamoudi KM; Aloraini T; Abdelhakim M; Althagafi AT; Kafkas S; Alsubaie L; Alrifai MT; Hoehndorf R; Alfares A; Alfadhel M Clin Genet; 2020 Dec; 98(6):555-561. PubMed ID: 32869858 [TBL] [Abstract][Full Text] [Related]
11. A novel pathogenic variant in the 3' end of the AGTPBP1 gene gives rise to neurodegeneration without cerebellar atrophy: an expansion of the disease phenotype? Türay S; Eröz R; Başak AN Neurogenetics; 2021 May; 22(2):127-132. PubMed ID: 33909173 [TBL] [Abstract][Full Text] [Related]
12. Exome sequencing reveals a novel CWF19L1 mutation associated with intellectual disability and cerebellar atrophy. Evers C; Kaufmann L; Seitz A; Paramasivam N; Granzow M; Karch S; Fischer C; Hinderhofer K; Gdynia G; Elsässer M; Pinkert S; Schlesner M; Bartram CR; Moog U Am J Med Genet A; 2016 Jun; 170(6):1502-9. PubMed ID: 27016154 [TBL] [Abstract][Full Text] [Related]
13. Homozygous GRID2 missense mutation predicts a shift in the D-serine binding domain of GluD2 in a case with generalized brain atrophy and unusual clinical features. Ali Z; Zulfiqar S; Klar J; Wikström J; Ullah F; Khan A; Abdullah U; Baig S; Dahl N BMC Med Genet; 2017 Dec; 18(1):144. PubMed ID: 29207948 [TBL] [Abstract][Full Text] [Related]
14. A homozygous potentially pathogenic variant in the PAXBP1 gene in a large family with global developmental delay and myopathic hypotonia. Alharby E; Albalawi AM; Nasir A; Alhijji SA; Mahmood A; Ramzan K; Abdusamad F; Aljohani A; Abdelsalam O; Eldardear A; Basit S Clin Genet; 2017 Dec; 92(6):579-586. PubMed ID: 28542722 [TBL] [Abstract][Full Text] [Related]