Newborn and carrier screening for spinal muscular atrophy-Reference-Cited by-同舟云学术

Newborn and carrier screening for spinal muscular atrophy

Published:2010-05-07 Issue:7 Volume:152A Page:1608-1616
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Prior Thomas W.,Snyder Pamela J.,Rink Britton D.,Pearl Dennis K.,Pyatt Robert E.,Mihal David C.,Conlan Todd,Schmalz Betsy,Montgomery Laura,Ziegler Katie,Noonan Carolee,Hashimoto Sayaka,Garner Shannon

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.33474/fullpdf

Reference38 articles.

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2. Determination of SMN1 and SMN2 copy number using Taqman technology;Anhuf;Hum Mutat,2003

3. Phenylbutyrate increases SMN gene expression in spinal muscular atrophy Patients;Brahe;Eur J Hum Genet,2005

4. In vivo activation of SMN in spinal muscular atrophy carriers and patients treated with valproate;Brichita;Ann Neurol,2006

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