CNM

Order number: GSD176
€48.79

VAT incl.

Application: a) Carrier identification in offspring after mating of a 'CNM-carrier' with a 'CNM-free' animal, b) Differential diagnosis in cases of clinical muscle insufficiency. Centronuclear Myopathy (CNM), also described as HMLR, or Hereditary Myopathy of Labrador Retrievers, has an autosomal recessive expression. Affected animals show insufficient muscle function resulting in various... more
Product information "CNM"
Application:
a) Carrier identification in offspring after mating of a 'CNM-carrier' with a 'CNM-free' animal,
b) Differential diagnosis in cases of clinical muscle insufficiency.
Centronuclear Myopathy (CNM), also described as HMLR, or Hereditary Myopathy of Labrador Retrievers, has an autosomal recessive expression. Affected animals show insufficient muscle function resulting in various clinical symptoms.
In the lexicon you will find more information and explanations about the article more
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Classification:
Type: DNA tests
Species: Dog
Class: Inherited diseases
Breeding clubs: Deutscher Retriever Club e.V., DRC. DNA-Programm Identität und Eigenschaften
Breed: Deutsche Dogge, Labrador Retriever, Mischling Hund, Sonstige, unbekannt, verschiedene Rassen
Group: Musculoskeletal system
P1-DRC - Labrador Retriever Bundle A
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Labrador Retriever Bundle B (P3)
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Copper storage tox. Labrador type [p]
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A – Locus / Agouti - DOG
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B – Locus (Coat color 'Brown' - DOG)
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crd-PRA
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Curly Coat
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D – Locus (Dilution)
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Cerebellar hypolasia (Dandy Walker Like...
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E – Locus (Coat color 'Yellow')
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Furnishings
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Glykogen storage disease GSDIIIa
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Golden Retriever PRA 1
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Golden Retriever PRA 2
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Harlekin coat pattern
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L – Locus (hair length)
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K – Locus
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Malignant Hyperthermia
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Merle coat pattern
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Narcolepsia (Dachshund)
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Narcolepsia (Labrador)
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Neuronal Ceroid-Lipofuszinosis 1 (Dachshund)
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Neuronal Ceroid-Lipofuszinosis 2 (Dachshund)
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Neuronal Ceroid-Lipofuszinosis 5(Golden Retriever)
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Osteogenesis Imperfecta (Dachshund)
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S – Locus (Piebald)
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Skeletal Dysplasia 2
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Von-Willebrand-Disease Type 1
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Golden Retriever muscular dystrophy
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Cystinurie Typ I-A
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cord1_crd4-PRA
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JME, Myoklonische Epilepsie Rhodesian Ridgeback
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IVDD-Type 1
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prcd-PRA***
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HNPK
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Exercise Induced Collapse (EIC)***
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Ichtyosis (ICT-A)***
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Collie eye anomaly (CEA)***
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Degenerative Myelopathy (DM)***
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RD_OSD***
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STGD - Stargardt Disease
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Hämophilie B [p]
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DNA profile Identity DOG (ISAG-22-Marker)
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DNA profile Identity DOG - *** class, extended...
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