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5 in total

1. Expansion of the myotonic dystrophy CTG repeat reduces expression of the flanking DMAHP gene.

Authors: C A Thornton; J P Wymer; Z Simmons; C McClain; R T Moxley
Journal: Nat Genet Date: 1997-08 Impact factor: 38.330

2. Myotonic dystrophy mutation: an unstable CTG repeat in the 3' untranslated region of the gene.

Authors: M Mahadevan; C Tsilfidis; L Sabourin; G Shutler; C Amemiya; G Jansen; C Neville; M Narang; J Barceló; K O'Hoy
Journal: Science Date: 1992-03-06 Impact factor: 47.728

3. Ciliary and retinal changes in myotonic dystrophy.

Authors: S Hayasaka; M Kiyosawa; S Katsumata; M Honda; S Takase; K Mizuno
Journal: Arch Ophthalmol Date: 1984-01

4. Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3' end of a transcript encoding a protein kinase family member.

Authors: J D Brook; M E McCurrach; H G Harley; A J Buckler; D Church; H Aburatani; K Hunter; V P Stanton; J P Thirion; T Hudson
Journal: Cell Date: 1992-02-21 Impact factor: 41.582

5. Characterization of the expression of DMPK and SIX5 in the human eye and implications for pathogenesis in myotonic dystrophy.

Authors: C L Winchester; R K Ferrier; A Sermoni; B J Clark; K J Johnson
Journal: Hum Mol Genet Date: 1999-03 Impact factor: 6.150

5 in total

1 in total

1. Polypoidal choroidal vasculopathy in a patient with DMPK-associated myotonic dystrophy.

Authors: Yuka Iida; Takaaki Hayashi; Teruaki Tokuhisa; Kei Mizobuchi; Shusaku Omoto; Tadashi Nakano
Journal: Doc Ophthalmol Date: 2022-03-13 Impact factor: 1.854

1 in total