Heterozygous FA2H mutations in autism spectrum disorders

Overview of attention for article published in BMC Medical Genomics, December 2013

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Heterozygous FA2H mutations in autism spectrum disorders 自閉症スペクトラム障害におけるヘテロ接合FA2H変異 http://t.co/0VHIg6zPAS #bmcmedicalgenetics

No evidence that FA2H plays a role in #autism spectrum, but other genes related to myelin synthesis shld be screened http://t.co/0z9QfNsYf2

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