Kinslow Tubb4a Foundation Inc
Our mission is to provide information on accessible and equitable treatment options for every child affected by TUBB4A-related leukodystrophy, regardless of their geographical location or socioeconomic status. We are committed to relentlessly pursuing research, collaboration, and advocacy to ensure that no child's journey is defined by limitations, but rather by possibilities for a healthier and brighter future.
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Kinslow TUBB4A Foundation A Disease May Be Rare But Hope Should Not Be Thank you for joining us in our fight. What is TUBB4A. TUBB4A is a gene responsible for encoding a protein called tubulin beta4A which plays a crucial role in the structure and function of microtubules essential components of cell architecture. Global Impact of TUBB4A TUBB4A mutations have a global impact on individuals and families contributing to various neurological disorders such as dystonia and hypomyelination.
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