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Canine RPGRIP1 mutation establishes cone-rod dystrophy in miniature longhaired dachshunds as a homologue of human Leber congenital amaurosis.

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Characterization of the COMMD1 (MURR1) mutation causing copper toxicosis in Bedlington terriers.

Animal genetics·2005

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Monoallelic loss-of-function variants in ZNF536 are associated with a neurodevelopmental disorder with prominent behavioral features.

American journal of human genetics·2026

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Science advances·2026

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Human reproduction update·2026

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Canine genetic disease: the beginning of the end?

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Canine RPGRIP1 mutation establishes cone-rod dystrophy in miniature longhaired dachshunds as a homologue of human Leber congenital amaurosis.

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