Filters: Author is Leal, Suzanne M [Clear All Filters]
A common X-linked inborn error of carnitine biosynthesis may be a risk factor for nondysmorphic autism.. Proceedings of the National Academy of Sciences of the United States of America. 109(21):7974-81.. 2012.
Chromosome 19p13 loci in Finnish migraine with aura families.. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics. 132B(1):85-9.. 2005.
A susceptibility locus for migraine with aura, on chromosome 4q24.. American journal of human genetics. 70(3):652-62.. 2002.