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Glykogenspeicherkrankheit II (GSDII) oder Pompe-Krankheit Einzelanalyse Vererbung: autosomal dominant

SKU: 61795843037
4.8

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Description

Vererbung: autosomal dominant

since at dominates over a

Even dogs that are double cryptic merle (Mc/Mc) can look inconspicuously like non-merle dogs

nervousness…) and incontinence alone or in combination with uncontrolled defecation

FREE ISAG 2020 DNA profile for identity and parentage verification

Glykogenspeicherkrankheit II (GSDII) oder Pompe-Krankheit Einzelanalyse Vererbung: autosomal dominantGlycogen storage diseases (GSD) are a group of autosomal recessive disorders of glycogen metabolism that occur in all species and result in glycogen accumulation in tissue and disturbed glucose homeostasis. The disease is characterized by a deficiency in glycogen debranching enzymes. Dogs affected with glycogen storage disease type II show esophageal dilation induced vomiting, progressive muscular weakness, clinical heart disease, and myocardial

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