Hypomorphic variants of cationic amino acid transporter 3 in males with autism spectrum disorders.

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Exome Sequencing Fails to Identify the Genetic Cause of Aicardi Syndrome.Advanced glycation endproducts, dityrosine and arginine transporter dysfunction in autism - a source of biomarkers for clinical diagnosis.

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Hypomorphic variants of cationic amino acid transporter 3 in males with autism spectrum disorders.

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http://www.wikidata.org/entity/Q36249309

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Hypomorphic variants of cation ...... ith autism spectrum disorders.

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Hypomorphic variants of cation ...... ith autism spectrum disorders.

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Hypomorphic variants of cation ...... ith autism spectrum disorders.

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Hypomorphic variants of cation ...... ith autism spectrum disorders.

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Hypomorphic variants of cation ...... ith autism spectrum disorders.

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Hypomorphic variants of cation ...... ith autism spectrum disorders.

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P1476

Hypomorphic variants of cation ...... ith autism spectrum disorders.

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Agnès Rastetter

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Anne Faudet

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Aurélia Jacquette

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Boris Keren

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Caroline Nava

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Christel Depienne

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Claire Amiet

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Claudine Laurent

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Cyril Mignot

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Céline Dupuits

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P2860

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Neuron-specific expression of cationic amino acid transporter 3 in the adult rat brain

Mutation screening of FOXP2 in individuals diagnosed with autistic disorder

A forkhead-domain gene is mutated in a severe speech and language disorder

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s00726-015-2057-3

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2647-2658

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scholarly article

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10.1007/S00726-015-2057-3

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Ellen I Closs

Anne Philippe

A Brice

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2015-07-28T00:00:00Z

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280536756

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26215737

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Autism spectrum

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4633447

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Hypomorphic variants of cationic amino acid transporter 3 in males with autism spectrum disorders.

about

P2860

P2860

Hypomorphic variants of cationic amino acid transporter 3 in males with autism spectrum disorders.

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