The
SMA registry is a database of genetic and clinical information for individuals
affected by Spinal Muscular Atrophy (SMA) and/or family members of individuals affected by SMA.
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Latest Events
News

A Malaysian In Florida Series
October 16, 2017

Living Life in The Face of Muscular Atrophy
October 29, 2017

SMA on Rare Disease Day on AFO LIVE
February 28, 2018
International Women’s Day 2018
March 8, 2018
My Birthday Wish – to Play Chinese Chess
March 18, 2018

Rare Disease Day, Honoring The Siblings
April 10, 2018

Battles Fought with Lots of Love
April 10, 2018

Founders, Edmund and Sook Yee
April 20, 2018


