ADA2 deficiency due to a novel structural variation in 22q11.1

Alice Grossi; Roberto Cusano; Marta Rusmini; Federica Penco; Francesca Schena; Rosa A Podda; Roberta Caorsi; Marco Gattorno; Paolo Uva; Isabella Ceccherini

doi:10.1111/cge.13518

ADA2 deficiency due to a novel structural variation in 22q11.1

Alice Grossi, Roberto Cusano, Marta Rusmini, Federica Penco, Francesca Schena, Rosa A Podda, Roberta Caorsi, Marco Gattorno, Paolo Uva, Isabella Ceccherini

Istituto "Giannina Gaslini"

Research output: Contribution to journal › Article

Original language	English
Pages (from-to)	732-733
Number of pages	2
Journal	Clinical Genetics
Volume	95
Issue number	6
DOIs	https://doi.org/10.1111/cge.13518
Publication status	Published - Jun 2019

Access to Document

10.1111/cge.13518

Cite this

Grossi, A., Cusano, R., Rusmini, M., Penco, F., Schena, F., Podda, R. A., Caorsi, R., Gattorno, M., Uva, P., & Ceccherini, I. (2019). ADA2 deficiency due to a novel structural variation in 22q11.1. Clinical Genetics, 95(6), 732-733. https://doi.org/10.1111/cge.13518

@article{460c5ca4c5114b28af0be31442cd9995,

title = "ADA2 deficiency due to a novel structural variation in 22q11.1",

author = "Alice Grossi and Roberto Cusano and Marta Rusmini and Federica Penco and Francesca Schena and Podda, {Rosa A} and Roberta Caorsi and Marco Gattorno and Paolo Uva and Isabella Ceccherini",

year = "2019",

month = jun,

doi = "10.1111/cge.13518",

language = "English",

volume = "95",

pages = "732--733",

journal = "Clinical Genetics",

issn = "0009-9163",

publisher = "Wiley-Blackwell Publishing Ltd",

number = "6",

}

TY - JOUR

T1 - ADA2 deficiency due to a novel structural variation in 22q11.1

AU - Grossi, Alice

AU - Cusano, Roberto

AU - Rusmini, Marta

AU - Penco, Federica

AU - Schena, Francesca

AU - Podda, Rosa A

AU - Caorsi, Roberta

AU - Gattorno, Marco

AU - Uva, Paolo

AU - Ceccherini, Isabella

PY - 2019/6

Y1 - 2019/6

U2 - 10.1111/cge.13518

DO - 10.1111/cge.13518

M3 - Article

C2 - 30920658

VL - 95

SP - 732

EP - 733

JO - Clinical Genetics

JF - Clinical Genetics

SN - 0009-9163

IS - 6

ER -