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Article

Mutation analysis and prenatal diagnosis of a family with Griscelli syndrome type 2: two novel mutations in the RAB27A gene.

World journal of pediatrics : WJP - 1 Aug 2017

Yeetong Patra, Suphapeetiporn Kanya, Shotelersuk Vorasuk

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PMID: 28484936
DOI: 10.1007/s12519-017-0037-2

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Mutation analysis and prenatal diagnosis of a family with Griscelli syndrome type 2: two novel mutations in the RAB27A gene.PMID 28484936Read ↗

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Evidence that Griscelli Syndrome with Neurological Involvement Is Caused by Mutations in RAB27A, Not MYO5ASemantic proximity Read ↗

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