Heterozygous PDGFRB Mutation in a Three-generation Family with Autosomal Dominant Infantile Myofibromatosis-Reference-Cited by-同舟云学术

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Heterozygous PDGFRB Mutation in a Three-generation Family with Autosomal Dominant Infantile Myofibromatosis

Published:2017 Issue:7 Volume:97 Page:858-859
ISSN:0001-5555
Container-title:Acta Dermato Venereologica
language:en
Short-container-title:Acta Derm Venerol

Author:

Lepelletier C,Al-Sarraj Y,Bodemer C,Shaath H,Fraitag S,Kambouris M,Hamel-Teillac D,Shanti H,Hadj-Rabia S

Publisher

Medical Journals Sweden AB

Subject

Dermatology,General Medicine

Cited by 15 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. Autosomal dominant multicentric infantile myofibromatosis: A case report;Pediatric Hematology Oncology Journal;2024-12

2. Late Relapse in Genetically Determined Infantile Myofibromatosis. A Case Report and Brief Focus on Recurrences;Journal of Pediatric Hematology/Oncology;2024-08-14

3. Clinical and molecular response to dasatinib in an adult patient with Penttinen syndrome;American Journal of Medical Genetics Part A;2021-12-11

4. PDGF receptor mutations in human diseases;Cellular and Molecular Life Sciences;2021-01-15

5. Major response to imatinib and chemotherapy in a newborn patient prenatally diagnosed with generalized infantile myofibromatosis;Pediatric Blood & Cancer;2020-09-08

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