Primary episodic ataxias are autosomal dominant channelopathies that manifest as attacks
of imbalance and incoordination. Mutations in two genes, KCNA1 and CACNA1A, cause the …

THEODORE D. GRAVES INTRODUCTION IN A RECENT PAPER BY GOODENOUGH
(1964), a distinction is made between the" phenomenal order" of observable vents and their …

Abstract REPORTS ON A COMPREHENSIVE TUDY OF DEVIANT BEHAVIOR,
ESPECIALLY EXCESSIVE ALCOHOL USE, IN A SMALL RURAL COMMUNITY …

The phenomenal growth in rural-to-urban migration during the post-World War II period is
matched by the growth of anthropological interest in this phenomenon: the trickle of migrant …

Gross ethnic differences in excessive drinking and other forms of social‐problem behavior
among Indians, Spanish‐Americans, and Anglo‐Americans living in a single Southwestern …

Proxemics is the study of how man structures microspace, how he relates physically to other
persons with whom he is interacting, and what is communicated by these physical …

Summary Background The Epilepsy Genetics (EPIGEN) Consortium was established to
undertake genetic mapping analyses with augmented statistical power to detect variants that …

Ion channels are membrane-bound proteins that perform key functions in virtually all human
cells. Such channels are critically important for the normal function of the excitable tissues of …

Heterozygous mutations in KMT2B are associated with an early-onset, progressive and
often complex dystonia (DYT28). Key characteristics of typical disease include focal motor …

Mutations in CACNA1A, which encodes the principal subunit of the P/Q calcium channel,
underlie episodic ataxia type 2 (EA2). In addition, some patients with episodic ataxia …