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About this Biochemistry, Genetics and Molecular Biology article

Malan syndrome in a patient with 19p13.2p13.12 deletion encompassing NFIX and CACNA1A genes: Case report and review of the literature by Bellucco, Fernanda T.; Mello, Claudia B.; Meloni, Vera A.; Melaragno, Maria Isabel is a Biochemistry, Genetics and Molecular Biology article available to read on EtoBox.

It is typically read by researchers, students, and practitioners in Biochemistry, Genetics and Molecular Biology.

Author
Bellucco, Fernanda T.; Mello, Claudia B.; Meloni, Vera A.; Melaragno, Maria Isabel
Publisher
Wiley (John Wiley & Sons); John Wiley and Sons Inc.; Wiley (ISSN 2324-9269)
Published
2019
Field
Biochemistry, Genetics and Molecular Biology (Life Sciences)

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