A recurrent mutation, ala391glu, in the transmembrane region of FGFR3 causes Crouzon syndrome and acanthosis nigricans (Q33677764)
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Current Data About A recurrent mutation, ala391glu, in the transmembrane region of FGFR3 causes Crouzon syndrome and acanthosis nigricans
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(P1476) "A recurrent mutation, ala391glu, in the transmembrane region of FGFR3 causes Crouzon syndrome and acanthosis nigricans" (language: en)
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P Rutland
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L J Pulleyn
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W Reardon
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C Moss
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J P Ellis
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R M Winter
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S Malcolm
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(P356) 10.1136/JMG.33.9.744
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