Tyler Izat

Affiliations

Center for Rare Childhood Disorders, Translational Genomics Research Institute, Phoenix, AZ, USA.

Publications (1)

Compound heterozygous mutations in SNAP29 is associated with Pelizaeus-Merzbacher-like disorder (PMLD).

Human genetics

Avec: Lorida Llaci , Keri Ramsey , Newell Belnap , Ana M Claasen , Chris D Balak , Szabolcs Szelinger , Wayne M Jepsen , Ashley L Siniard , Ryan Richholt , Tyler Izat , Marcus Naymik , Matt De Both , Ignazio S Piras , David W Craig , Matthew J Huentelman , Vinodh Narayanan , Isabelle Schrauwen , Sampathkumar Rangasamy

Réseau de co-auteurs

Lorida Llaci 1 collaboration

Keri Ramsey 1 collaboration

Newell Belnap 1 collaboration

Ana M Claasen 1 collaboration

Chris D Balak 1 collaboration

Szabolcs Szelinger 1 collaboration

Wayne M Jepsen 1 collaboration

Ashley L Siniard 1 collaboration

Ryan Richholt 1 collaboration

Marcus Naymik 1 collaboration

Matt De Both 1 collaboration

Ignazio S Piras 1 collaboration

David W Craig 1 collaboration

Matthew J Huentelman 1 collaboration

Vinodh Narayanan 1 collaboration

Isabelle Schrauwen 1 collaboration

Sampathkumar Rangasamy 1 collaboration