<p>Supporting dataset for a publication in Genome Biology, entitled</p> <p>"KIAA0556 is a novel ciliary basal body component mutated in Joubert syndrome" .</p> <p> </p
Joubert syndrome (JS) and related disorders are a group of autosomal-recessive conditions sharing th...
Joubert syndrome (JS) is a mendelian disease that falls into the category of cerebellar and brainste...
Joubert syndrome (JS) is a recessive neurodevelopmental disorder characterized by hypotonia, ataxia,...
Supporting dataset for a publication in Genome Biology, entitled "KIAA0556 is a novel ciliary basal...
Contains fulltext : 155320.pdf (publisher's version ) (Open Access)Defective prima...
Contains fulltext : 152408.pdf (publisher's version ) (Open Access)BACKGROUND: Jou...
Contains fulltext : 167861.pdf (publisher's version ) (Closed access)Joubert Syndr...
Joubert syndrome (JS) is a recessive neurodevelopmental disorder characterized by a distinctive mid-...
Results of the SF-TAP analysis with over-expressed N-terminally SF-TAP-tagged KIAA0556 in HEK293T ce...
Supplementary information to the data in Fig. 8 . a Schematic representation of all the different ...
Contains fulltext : 70259.pdf (publisher's version ) (Closed access)Joubert syndro...
Abstract Background KIAA0586, also known as Talpid3, plays critical roles in primary cilia formation...
Objective: Joubert syndrome is a neurodevelopmental disorder with a distinctive hindbrain malformati...
BACKGROUND: Joubert syndrome (JS) is a recessive ciliopathy characterised by a distinctive brain mal...
Background: Joubert syndrome (JBS) is a rare neurodevelopmental disorder associated with progressive...
Joubert syndrome (JS) and related disorders are a group of autosomal-recessive conditions sharing th...
Joubert syndrome (JS) is a mendelian disease that falls into the category of cerebellar and brainste...
Joubert syndrome (JS) is a recessive neurodevelopmental disorder characterized by hypotonia, ataxia,...
Supporting dataset for a publication in Genome Biology, entitled "KIAA0556 is a novel ciliary basal...
Contains fulltext : 155320.pdf (publisher's version ) (Open Access)Defective prima...
Contains fulltext : 152408.pdf (publisher's version ) (Open Access)BACKGROUND: Jou...
Contains fulltext : 167861.pdf (publisher's version ) (Closed access)Joubert Syndr...
Joubert syndrome (JS) is a recessive neurodevelopmental disorder characterized by a distinctive mid-...
Results of the SF-TAP analysis with over-expressed N-terminally SF-TAP-tagged KIAA0556 in HEK293T ce...
Supplementary information to the data in Fig. 8 . a Schematic representation of all the different ...
Contains fulltext : 70259.pdf (publisher's version ) (Closed access)Joubert syndro...
Abstract Background KIAA0586, also known as Talpid3, plays critical roles in primary cilia formation...
Objective: Joubert syndrome is a neurodevelopmental disorder with a distinctive hindbrain malformati...
BACKGROUND: Joubert syndrome (JS) is a recessive ciliopathy characterised by a distinctive brain mal...
Background: Joubert syndrome (JBS) is a rare neurodevelopmental disorder associated with progressive...
Joubert syndrome (JS) and related disorders are a group of autosomal-recessive conditions sharing th...
Joubert syndrome (JS) is a mendelian disease that falls into the category of cerebellar and brainste...
Joubert syndrome (JS) is a recessive neurodevelopmental disorder characterized by hypotonia, ataxia,...