Phacomatosis pigmentovascularis spilorosea and mutation in the <i>PTPN11</i> gene: new case with significant neurologic impairment-Reference-Cited by-同舟云学术

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Phacomatosis pigmentovascularis spilorosea and mutation in the PTPN11 gene: new case with significant neurologic impairment

Published:2022-06-14 Issue:8 Volume:20 Page:1133-1136
ISSN:1610-0379
Container-title:JDDG: Journal der Deutschen Dermatologischen Gesellschaft
language:en
Short-container-title:J Deutsche Derma Gesell

Author:

Maione Vincenzo¹,Soglia Simone¹,Miccio Laura¹,Calzavara‐Pinton Piergiacomo¹²,Napolitano Angela³,Cinquina Valeria⁴,Ritelli Marco⁴,Colombi Marina⁴

Affiliation:

1. Division of Dermatology ASST Spedali Civili di Brescia Brescia Italy

2. Division of Dermatology Department of Clinical and Experimental Sciences University of Brescia Brescia Italy

3. Division of Radiology ASST Papa Giovanni XIII Bergamo Italy

4. Division of Biology and Genetics Department of Molecular and Translational Medicine University of Brescia Brescia Italy

Publisher

Wiley

Subject

Dermatology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/ddg.14786

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Somatic GNA11/GNAQ variants in a cohort of Chinese children with phakomatosis pigmentovascularis;Pediatric Investigation;2024-04-17

2. Genetic and phenotypic diversities of nevus spilus phenotypes: Case series and a proposed diagnostic algorithm;Clinical Genetics;2023-07-27

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