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A Patient With the Simpson-Golabi-Behmel Syndrome Displays a Loss-of-Function Point Mutation in GPC3 That Inhibits the Attachment of this Proteoglycan to the Cell Surface

AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2009)

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AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Volume 149A, Issue 3, Pages 552-554

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WILEY

DOI: 10.1002/ajmg.a.32669

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A Patient With the Simpson-Golabi-Behmel Syndrome Displays a Loss-of-Function Point Mutation in GPC3 That Inhibits the Attachment of this Proteoglycan to the Cell Surface

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AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Publisher

WILEY

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A Patient With the Simpson-Golabi-Behmel Syndrome Displays a Loss-of-Function Point Mutation in GPC3 That Inhibits the Attachment of this Proteoglycan to the Cell Surface

Journal

AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Publisher

WILEY

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