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Neurofibromatosis Type Probe

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Cat.No.
FMDC-27
Description
Neurofibromatosis type 1 (NF1) is a common autosomal dominant disorder characterised by neurofibromas, café-au-lait spots, freckles, Lisch nodules, bone deformities, learning disabilities, macrocephaly, short stature and predisposition to developing tumors such as myeloid malignancies, gliomas and pheochromocytomas and occurs in 1 in 3,000-4,000 people. This is caused by mutations of the tumour suppressor gene NF1.
Size
5 Tests, 10 Tests
Label
Red/Green
Locus
17p
Specificity
Human
Usage
warningFor Research Use Only. Not for use in diagnostic procedures.
Storage
Store at minus 20 centigrade
Citation Guidance
If you use this products in your scientific publication, it should be cited in the publication as: Creative Bioarray cat no. If your paper has been published, please click here to submit the PubMed ID of your paper to get a coupon.

For research use only. Not for any other purpose.

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