Choreoathetosis is a major clinical feature in only a small number of hereditary neurological disorders. We define a new X-linked syndrome with a unique clinical picture characterized by mild mental retardation, choreoathetosis, and abnormal behavior. We mapped the disease in a four- generation pedigree to chromosome Xp11 by linkage analysis and defined a candidate region containing a number of genes possibly involved in neuronal signaling, including a potassium channel gene and a neuronal G protein- coupled receptor.SCOPUS: ar.jinfo:eu-repo/semantics/publishe
Contains fulltext : 166935.pdf (Publisher’s version ) (Closed access)Nonsyndromic ...
Paroxysmal kinesigenic choreoathetosis (PKC) is a rare paroxysmal movement disorder characterized by...
International audienceTen percent of cases of intellectual deficiency in boys are caused by genes lo...
Choreoathetosis is a major clinical feature in only a small number of hereditary neurological disord...
SummaryChoreoathetosis is a major clinical feature in only a small number of hereditary neurological...
SummaryBenign infantile familial convulsions is an autosomal dominant disorder characterized by nonf...
Benign infantile familial convulsions is an autosomal dominant disorder characterized by nonfebrile ...
International audienceLinkage analysis was performed in three generations of a French family segrega...
Genetic abnormalities frequently give rise to a mental retardation phenotype. Recent advances in res...
Contains fulltext : 47374.pdf (publisher's version ) (Closed access)Genetic factor...
Contains fulltext : 50817.pdf (publisher's version ) (Closed access)The extensive ...
International audienceFried syndrome, first described in 1972, is a rare X-linked mental retardation...
Objective: To describe a new syndrome of X-linked myoclonic epilepsy with generalized spasticity and...
International audiencePurpose: WNK3 kinase (PRKWNK3) has been implicated in the development and func...
Classification of neuropathies into Charcot-Marie-Tooth syndrome (CMT, hereditary motor and sensory ...
Contains fulltext : 166935.pdf (Publisher’s version ) (Closed access)Nonsyndromic ...
Paroxysmal kinesigenic choreoathetosis (PKC) is a rare paroxysmal movement disorder characterized by...
International audienceTen percent of cases of intellectual deficiency in boys are caused by genes lo...
Choreoathetosis is a major clinical feature in only a small number of hereditary neurological disord...
SummaryChoreoathetosis is a major clinical feature in only a small number of hereditary neurological...
SummaryBenign infantile familial convulsions is an autosomal dominant disorder characterized by nonf...
Benign infantile familial convulsions is an autosomal dominant disorder characterized by nonfebrile ...
International audienceLinkage analysis was performed in three generations of a French family segrega...
Genetic abnormalities frequently give rise to a mental retardation phenotype. Recent advances in res...
Contains fulltext : 47374.pdf (publisher's version ) (Closed access)Genetic factor...
Contains fulltext : 50817.pdf (publisher's version ) (Closed access)The extensive ...
International audienceFried syndrome, first described in 1972, is a rare X-linked mental retardation...
Objective: To describe a new syndrome of X-linked myoclonic epilepsy with generalized spasticity and...
International audiencePurpose: WNK3 kinase (PRKWNK3) has been implicated in the development and func...
Classification of neuropathies into Charcot-Marie-Tooth syndrome (CMT, hereditary motor and sensory ...
Contains fulltext : 166935.pdf (Publisher’s version ) (Closed access)Nonsyndromic ...
Paroxysmal kinesigenic choreoathetosis (PKC) is a rare paroxysmal movement disorder characterized by...
International audienceTen percent of cases of intellectual deficiency in boys are caused by genes lo...