A null mutation in the rhodopsin gene causes rod photoreceptor dysfunction and autosomal recessive retinitis pigmentosa.

Rhodopsin mutations in autosomal dominant retinitis pigmentosa.

Identification of a rhodopsin gene mutation in a large family with autosomal dominant retinitis pigmentosa.

Pro-347-Arg mutation of the rhodopsin gene in autosomal dominant retinitis pigmentosa.

Mutation spectrum of the rhodopsin gene among patients with autosomal dominant retinitis pigmentosa.

SLC7A14 linked to autosomal recessive retinitis pigmentosa.

A 3-bp deletion in the rhodopsin gene in a family with autosomal dominant retinitis pigmentosa.

Identification of the Photoreceptor Transcriptional Co-Repressor SAMD11 as Novel Cause of Autosomal Recessive Retinitis Pigmentosa.

Autosomal dominant retinitis pigmentosa (ADRP): a rhodopsin mutation in a Scottish family.

Transgenic mice with a rhodopsin mutation (Pro23His): a mouse model of autosomal dominant retinitis pigmentosa.

Doyne Lecture. Rhodopsin and autosomal dominant retinitis pigmentosa.

Homozygosity mapping reveals new nonsense mutation in the FAM161A gene causing autosomal recessive retinitis pigmentosa in a Palestinian family.

A six-generation family with autosomal dominant retinitis pigmentosa and a rhodopsin gene mutation (arginine-135-leucine).

Novel compound heterozygous mutation in the CNGA1 gene underlie autosomal recessive retinitis pigmentosa in a Chinese family.

A homozygous missense mutation in NEUROD1 is associated with nonsyndromic autosomal recessive retinitis pigmentosa.

Autosomal dominant retinitis pigmentosa with rhodopsin, valine-345-methionine.

Reduced rod electroretinograms in carrier parents of two Japanese siblings with autosomal recessive retinitis pigmentosa associated with PDE6B gene mutations.

Mutations within the rhodopsin gene in patients with autosomal dominant retinitis pigmentosa.

Gelsolin dysfunction causes photoreceptor loss in induced pluripotent cell and animal retinitis pigmentosa models.

Abnormal dark adaptation kinetics in autosomal dominant sector retinitis pigmentosa due to rod opsin mutation.

A point mutation of the rhodopsin gene in one form of retinitis pigmentosa.

Point mutations of rhodopsin gene found in Japanese families with autosomal dominant retinitis pigmentosa (ADRP).

Autosomal recessive posterior column ataxia with retinitis pigmentosa caused by novel mutations in the FLVCR1 gene.

Mutational Analysis of the Rhodopsin Gene in Sector Retinitis Pigmentosa.

A completed screen for mutations of the rhodopsin gene in a panel of patients with autosomal dominant retinitis pigmentosa.

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Rhodopsin mutations in autosomal dominant retinitis pigmentosa.

Identification of a rhodopsin gene mutation in a large family with autosomal dominant retinitis pigmentosa.

Pro-347-Arg mutation of the rhodopsin gene in autosomal dominant retinitis pigmentosa.

Mutation spectrum of the rhodopsin gene among patients with autosomal dominant retinitis pigmentosa.

SLC7A14 linked to autosomal recessive retinitis pigmentosa.

A 3-bp deletion in the rhodopsin gene in a family with autosomal dominant retinitis pigmentosa.

Identification of the Photoreceptor Transcriptional Co-Repressor SAMD11 as Novel Cause of Autosomal Recessive Retinitis Pigmentosa.

Autosomal dominant retinitis pigmentosa (ADRP): a rhodopsin mutation in a Scottish family.

Transgenic mice with a rhodopsin mutation (Pro23His): a mouse model of autosomal dominant retinitis pigmentosa.

Doyne Lecture. Rhodopsin and autosomal dominant retinitis pigmentosa.

Homozygosity mapping reveals new nonsense mutation in the FAM161A gene causing autosomal recessive retinitis pigmentosa in a Palestinian family.

A six-generation family with autosomal dominant retinitis pigmentosa and a rhodopsin gene mutation (arginine-135-leucine).

Novel compound heterozygous mutation in the CNGA1 gene underlie autosomal recessive retinitis pigmentosa in a Chinese family.

A homozygous missense mutation in NEUROD1 is associated with nonsyndromic autosomal recessive retinitis pigmentosa.

Autosomal dominant retinitis pigmentosa with rhodopsin, valine-345-methionine.

Reduced rod electroretinograms in carrier parents of two Japanese siblings with autosomal recessive retinitis pigmentosa associated with PDE6B gene mutations.

Mutations within the rhodopsin gene in patients with autosomal dominant retinitis pigmentosa.

Gelsolin dysfunction causes photoreceptor loss in induced pluripotent cell and animal retinitis pigmentosa models.

Abnormal dark adaptation kinetics in autosomal dominant sector retinitis pigmentosa due to rod opsin mutation.

A point mutation of the rhodopsin gene in one form of retinitis pigmentosa.

Point mutations of rhodopsin gene found in Japanese families with autosomal dominant retinitis pigmentosa (ADRP).

Autosomal recessive posterior column ataxia with retinitis pigmentosa caused by novel mutations in the FLVCR1 gene.

Mutational Analysis of the Rhodopsin Gene in Sector Retinitis Pigmentosa.

A completed screen for mutations of the rhodopsin gene in a panel of patients with autosomal dominant retinitis pigmentosa.

A null mutation in the rhodopsin gene causes rod photoreceptor dysfunction and autosomal recessive retinitis pigmentosa.

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