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Human Genetics
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Volume 138, May 2019, Issue 5, Pages 437-546
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1. Special issue on canine genetics: animal models for human disease and gene therapies, new discoveries for canine inherited diseases, and standards and guidelines for clinical genetic testing for domestic dogs
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Tác giả
Lisa G. Shaffer.
2. Natural models for retinitis pigmentosa: progressive retinal atrophy in dog breeds
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Tác giả
Morgane Bunel, Gilles Chaudieu, Christian Hamel, Laetitia Lagoutte.
3. Canine neuropathies: powerful spontaneous models for human hereditary sensory neuropathies
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Tác giả
Solenne Correard, Jocelyn Plassais, Laëtitia Lagoutte, Nadine Botherel.
4. Personalized medicine: going to the dogs?
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Tác giả
Katrina L. Mealey, Stephanie E. Martinez, Nicolas F. Villarino.
5. Gene therapies in canine models for Duchenne muscular dystrophy
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Tác giả
Peter P. Nghiem, Joe N. Kornegay.
6. Correction to: Gene therapies in canine models for Duchenne muscular dystrophy
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Tác giả
Peter P. Nghiem, Joe N. Kornegay.
7. Standards and guidelines for canine clinical genetic testing laboratories
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Tác giả
Lisa G. Shaffer, Kyle Sundin, Anja Geretschlaeger, Julia Segert.
8. Quality assurance checklist and additional considerations for canine clinical genetic testing laboratories: a follow-up to the published standards and guidelines
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Tác giả
Lisa G. Shaffer, Anja Geretschlaeger, Christina J. Ramirez.
9. A glycine transporter SLC6A5 frameshift mutation causes startle disease in Spanish greyhounds
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Tác giả
Sarah C. Murphy, Alfredo Recio, Cristian de la Fuente, Ling T. Guo.
10. A missense variant in the titin gene in Doberman pinscher dogs with familial dilated cardiomyopathy and sudden cardiac death
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Tác giả
Kathryn M. Meurs, Steven G. Friedenberg, Justin Kolb, Chandra Saripalli.
11. Canine models of human amelogenesis imperfecta: identification of novel recessive ENAM and ACP4 variants
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Tác giả
Marjo K. Hytönen, Meharji Arumilli, Eva Sarkiala, Pekka Nieminen.
12. A frameshift insertion in SGK3 leads to recessive hairlessness in Scottish Deerhounds: a candidate gene for human alopecia conditions
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Tác giả
Marjo K. Hytönen, Hannes Lohi.
13. Predicting copper toxicosis: relationship between the ATP7A and ATP7B gene mutations and hepatic copper quantification in dogs
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Tác giả
Sharon Pindar, Christina Ramirez.
