PodParley PodParley
PodParley
Rare Disease Groups Seeking Public Support To Renew Newborn Screening Act & Winter Hibernation episode artwork

EPISODE · Oct 21, 2019 · 5 MIN

Rare Disease Groups Seeking Public Support To Renew Newborn Screening Act & Winter Hibernation

from The Spinal Muscular Atrophy Podcast with Kevin Schaefer · host SMA News Today

Episode metadata supplied by the publisher feed · Published Oct 21, 2019

Embed this episode

Ready to play

Rare Disease Groups Seeking Public Support To Renew Newborn Screening Act & Winter Hibernation

0:00 5:49

No transcript for this episode yet

We transcribe on demand. Request one and we'll notify you when it's ready — usually under 10 minutes.

Share this episode

Similar Episodes

No similar episodes found.

Similar Podcasts

No similar podcasts found.

Frequently Asked Questions

How long is this episode of The Spinal Muscular Atrophy Podcast with Kevin Schaefer?

This episode is 5 minutes long.

When was this The Spinal Muscular Atrophy Podcast with Kevin Schaefer episode published?

This episode was published on October 21, 2019.

Can I download this The Spinal Muscular Atrophy Podcast with Kevin Schaefer episode?

Yes. Use the download control on the episode player to save the publisher-provided media file.
URL copied to clipboard!