Bayat, Allan <br/><br/>
PIGT-CDG, a disorder of the glycosylphosphatidylinositol anchor: description of 13 novel patients and expansion of the clinical characteristics.  [electronic resource] 

 -  Genetics in medicine : official journal of the American College of Medical Genetics  10 2019 
 - 2216-2223 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1530-0366 
<br/><br/><label>Standard No.: </label>10.1038/s41436-019-0512-3  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--genetics<br/>Acyltransferases--genetics<br/>Child<br/>Child, Preschool<br/>Developmental Disabilities--genetics<br/>Epilepsy--genetics<br/>Female<br/>Genetic Association Studies<br/>Genotype<br/>Glycosylphosphatidylinositols--deficiency<br/>Homozygote<br/>Humans<br/>Infant<br/>Infant, Newborn<br/>Male<br/>Mutation<br/>Pedigree<br/>Phenotype<br/>Seizures--genetics