Deletions in exon 5 of the human rhodopsin gene causing a shift in the reading frame and autosomal dominant retinitis pigmentosa.

M Horn; P Humphries; M Kunisch; C Marchese; E Apfelstedt-Sylla; L Fugi; E Zrenner; P Kenna; A Gal; J Farrar

doi:10.1007/BF00220073

Deletions in exon 5 of the human rhodopsin gene causing a shift in the reading frame and autosomal dominant retinitis pigmentosa.

Identifier:nobleid.org/w1/20260515/491FC2CC

Type:Journal Article

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Deletions in exon 5 of the human rhodopsin gene causing a shift in the reading frame and autosomal dominant retinitis pigmentosa.

Identifier:nobleid.org/w1/20260515/491FC2CC

Type:Journal Article

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