The PHF6 Mutation c.1A>G; pM1V Causes Börjeson-Forsman-Lehmann Syndrome in a Family with Four Affected Young Boys

Publisher： Karger

E-ISSN： 1661-8777|6|4|181-186

ISSN： 1661-8769

Source： Molecular Syndromology, Vol.6, Iss.4, 2015-0, pp. : 181-186

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