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UnknownLGI1 acts presynaptically to regulate excitatory synaptic transmission during early postnatal development.
Not available
S-EPMC4754946 | biostudies-literature
UnknownPLEKHG5 deficiency leads to an intermediate form of autosomal-recessive Charcot-Marie-Tooth disease.
Not available
S-EPMC3983407 | biostudies-literature
UnknownDepdc5 knockdown causes mTOR-dependent motor hyperactivity in zebrafish.
Not available
S-EPMC5945968 | biostudies-literature
UnknownA second locus for familial generalized epilepsy with febrile seizures plus maps to chromosome 2q21-q33.
Not available
S-EPMC1288241 | biostudies-literature
UnknownSecond-hit mosaic mutation in mTORC1 repressor DEPDC5 causes focal cortical dysplasia-associated epilepsy.
Not available
S-EPMC5983335 | biostudies-literature
UnknownMutations of DEPDC5 cause autosomal dominant focal epilepsies.
Not available
S-EPMC5010101 | biostudies-literature
UnknownInvolvement of ADGRV1 Gene in Familial Forms of Genetic Generalized Epilepsy.
Not available
S-EPMC8567843 | biostudies-literature
UnknownGenome-wide high-resolution aCGH analysis of gestational choriocarcinomas.
Not available
S-EPMC3253784 | biostudies-literature
UnknownSEPT9 gene sequencing analysis reveals recurrent mutations in hereditary neuralgic amyotrophy.
Not available
S-EPMC2683739 | biostudies-literature
UnknownShould ITSN1 be considered as a Mendelian Parkinson's disease gene? Description of three novel families.
Not available
S-EPMC12534528 | biostudies-literature
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