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UnknownSize does matter: 18 amino acids at the N-terminal tip of an amino acid transporter in Leishmania determine substrate specificity.
Not available
S-EPMC4637868 | biostudies-literature
UnknownA homozygous mutation in human PRICKLE1 causes an autosomal-recessive progressive myoclonus epilepsy-ataxia syndrome.
Not available
S-EPMC2668041 | biostudies-literature
UnknownNeuronal sodium-channel alpha1-subunit mutations in generalized epilepsy with febrile seizures plus.
Not available
S-EPMC1275639 | biostudies-literature
UnknownX-linked protocadherin 19 mutations cause female-limited epilepsy and cognitive impairment.
Not available
S-EPMC2756413 | biostudies-literature
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