Genetics of low spinal muscular atrophy carrier frequency in sub-Saharan Africa

Homozygous SMN2 deletion is a protective factor in the Swedish ALS population

(2012) Philippe Corcia et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Correlation of SMN2, NAIP, p44, H4F5 and Occludin genes copy number with spinal muscular atrophy phenotype in Tunisian patients

(2011) Abdelbasset Amara et al.   EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY

Population variation in NAIP functional copy number confers increased cell death upon Legionella pneumophila infection

(2011) Michele Boniotto et al.   HUMAN IMMUNOLOGY

Identification of bidirectional gene conversion between SMN1 and SMN2 by simultaneous analysis of SMN dosage and hybrid genes in a Chinese population

(2011) Tai-Heng Chen et al.   JOURNAL OF THE NEUROLOGICAL SCIENCES

Confidence intervals that match Fisher's exact or Blaker's exact tests

(2009) Michael P. Fay   BIOSTATISTICS

Differences in SMN1 allele frequencies among ethnic groups within North America

(2009) B C Hendrickson et al.   JOURNAL OF MEDICAL GENETICS

Consanguinity and reproductive health among Arabs

(2009) Ghazi O Tadmouri et al.   Reproductive Health

Regulation of SMN Protein Stability

(2008) B. G. Burnett et al.   MOLECULAR AND CELLULAR BIOLOGY