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Michael L Raff, MD

Michael L Raff, MD

Michael L Raff, MD

Genetics, Medical, Medical Genetics

Accepting New Patients

Virtual Visits Available

Phone: 253-403-3476    Fax: 253-403-8674

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Provider Details

Certification: American Board of Medical Genetics; American Board of Internal Medicine

Medical Association Memberships: American College of Medical Genetics American College of Physicians

Professional School: McGill University, Montreal, Quebec

Residency: Scripps Mercy Hospital, University of California, San Diego - Internal Med

Fellowship: University of Washington School of Medicine - Medical Genetics; Training Program

Internship: Royal Victoria Hospital, McGill University, Montreal, Quebec - Internal Med

Research & Publications

Zhan Q, Wang L, Xu X, Sun Y, Li L, Qi X, Chen F, Wei X, Raff ML, Yu P, Jin F. An APC Mutation in a Large Chinese Kindred With Familial Adenomatous Polyposis Was Identified Using Both Next Generation Sequencing and Simple STR Marker Haplotypes. Front Genet. 2020 Mar 4;11:191. doi: 10.3389/fgene.2020.00191. 

Khare S, Nick JA, Zhang Y, Galeano K, Butler B, Khoshbouei H, Rayaprolu S, Hathorn T, Ranum LPW, Smithson L, Golde TE, Paucar M, Morse R, Raff M, Simon J, Nordenskjöld M, Wirdefeldt K, Rincon-Limas DE, Lewis J, Kaczmarek LK, Fernandez-Funez P, Nick HS, Waters MF. A KCNC3 mutation causes a neurodevelopmental, non-progressive SCA13 subtype associated with dominant negative effects and aberrant EGFR trafficking. PLoS One. 2017 May 3;12(5):e0173565. doi: 10.1371/journal.pone.0173565. 

Learn more about ongoing studies and medical research at the MultiCare Institute for Research & Innovation.

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