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A recurrent de novo missense mutation in UBTF causes developmental neuroregression.
Hum Mol Genet. 2018 Feb 15;27(4):691-705. doi: 10.1093/hmg/ddx435.
Hum Mol Genet. 2018.
PMID: 29300972
Free PMC article.
A recurrent de novo missense mutation in UBTF causes developmental neuroregression.
Toro C, Hori RT, Malicdan MCV, Tifft CJ, Goldstein A, Gahl WA, Adams DR, Fauni HB, Wolfe LA, Xiao J, Khan MM, Tian J, Hope KA, Reiter LT, Tremblay MG, Moss T, Franks AL, Balak C; C4RCD Research Group; LeDoux MS.
Toro C, et al. Among authors: fauni hb.
Hum Mol Genet. 2018 Apr 1;27(7):1310. doi: 10.1093/hmg/ddy049.
Hum Mol Genet. 2018.
PMID: 29447355
Free PMC article.
No abstract available.
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Kilquist syndrome: A novel syndromic hearing loss disorder caused by homozygous deletion of SLC12A2.
Macnamara EF, Koehler AE, D'Souza P, Estwick T, Lee P, Vezina G; Undiagnosed Diseases Network; Fauni H, Braddock SR, Torti E, Holt JM, Sharma P, Malicdan MCV, Tifft CJ.
Macnamara EF, et al.
Hum Mutat. 2019 May;40(5):532-538. doi: 10.1002/humu.23722. Epub 2019 Mar 12.
Hum Mutat. 2019.
PMID: 30740830
Free PMC article.
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Genomic analysis, immunomodulation and deep phenotyping of patients with nodding syndrome.
Soldatos A, Nutman TB, Johnson T, Dowell SF, Sejvar JJ, Wilson MR, DeRisi JL, Inati SK, Groden C, Evans C, O'Connell EM, Toliva BO, Aceng JR, Aryek-Kwe J, Toro C, Stratakis CA, Buckler AG, Cantilena C, Palmore TN, Thurm A, Baker EH, Chang R, Fauni H, Adams D, Macnamara EF, Lau CC, Malicdan MCV, Pusey-Swerdzewski B, Downing R, Bunga S, Thomas JD, Gahl WA, Nath A.
Soldatos A, et al.
Brain. 2023 Mar 1;146(3):968-976. doi: 10.1093/brain/awac357.
Brain. 2023.
PMID: 36181424
Free PMC article.
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