Toggle navigation
PDFSEARCH.IO
Document Search Engine - browse more than 18 million documents
Sign up
Sign in
<--- Back to Details
First Page
Document Content
Date: 2014-12-04 01:13:45
Health
SMN1
Medical classification
Multiplex
LOINC
Laboratory techniques
Science
Health informatics
Laboratory Standards and Procedures Subcommittee Meeting September 16, 2010
Add to Reading List
Source URL: www.hrsa.gov
Download Document from Source Website
File Size: 24,79 KB
Share Document on Facebook
Similar Documents
npg Call in the backup The most common genetic killer of infants, a disease known as spinal muscular atrophy, is caused by mutations in a single gene. The human genome contains its own backup system—near-identical cop
DocID: 177oq - View Document
ISIS INITIATES PHASE 1 CLINICAL STUDY OF ISIS-SMNRX IN PATIENTS WITH SPINAL MUSCULAR ATROPHY U.S. FDA has granted both Fast Track Status and Orphan Drug Designation for ISIS-SMNRx CARLSBAD, Calif., December 19, 2011 –
DocID: 15Kdp - View Document
ISSNBiopolymers and CellVol. 26. N 1 Implementation of the quantitative Real-Time PCR for the molecular-genetic diagnostics of spinal muscular atrophy O. O. Soloviov, G. B. Livshits, S. S. Podlesnaya
DocID: 13lsk - View Document
BioMed Research International Special Issue on Motor Neuron Disorders: Molecular Mechanisms of Pathogenesis and Therapeutic Developments CALL FOR PAPERS
DocID: 12fvF - View Document
Gene Transfer Clinical Trial for Spinal Muscular Atrophy Type 1 This study is a phase I, single-site, dose escalation study to evaluate the safety and efficacy of gene transfer for Spinal Muscular Atrophy Type 1 (SMA1).
DocID: 11rVr - View Document