Talk:Tryptase

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Needs addition of ‘hereditary alpha tryptasaemia syndrome’ (HATS) to the Clinical Use section. I wasn’t sure how to word and reference it well enough to do so myself.

https://www.niaid.nih.gov/research/hereditary-alpha-tryptasemia-faq

Alpha tryptasemia / hereditary alpha tryptasemia syndrome[edit]

This new condition identified by the NIH is caused by one more more extra copies of the gene that encodes tryptase. It obviously needs to be added to this article, but I don’t feel qualified to do so. Zctyp18 (talk) 21:00, 6 October 2018 (UTC)[reply]