CHROMOSOME 19 :
- Myotonia dystrophica
- Insulin receptor gene
- NPHS 1 (Nephrin) - Congenital FINNISH type of Nephrotic Syndrome (AR)
NPHS 1 - Chromosome 19
NPHS 2 - Chromosome 1
Human Insulin gene - Chromosome 11
Insulin Receptor gene - Chromosome 19
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