<scp>SCALP</scp> syndrome with a germline heterozygous <i>DOCK6</i> mutation and somatic mosaic <i>NRAS</i> <scp>Q61R</scp> mutation-Reference-Cited by-同舟云学术

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SCALP syndrome with a germline heterozygous DOCK6 mutation and somatic mosaic NRAS Q61R mutation

Published:2022-12 Issue: Volume: Page:
ISSN:0736-8046
Container-title:Pediatric Dermatology
language:en
Short-container-title:Pediatric Dermatology

Author:

Meyer Summer N.¹^ORCID,Simmons Elanee M.¹,McPherson John D.²,Awasthi Smita¹³^ORCID,Kiuru Maija¹⁴^ORCID

Affiliation:

1. Department of Dermatology University of California Davis Sacramento California USA

2. Department of Biochemistry and Molecular Medicine University of California Davis Sacramento California USA

3. Department of Pediatrics University of California Davis Sacramento California USA

4. Department of Pathology & Laboratory Medicine University of California Davis Sacramento California USA

Publisher

Wiley

Subject

Dermatology,Pediatrics, Perinatology and Child Health

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/pde.15184

Reference22 articles.

1. Multiple Hamartomas Associated with Intracranial Malformation

2. SCALP syndrome: Sebaceous nevus syndrome, CNS malformations, aplasia cutis congenita, limbal dermoid, and pigmented nevus (giant congenital melanocytic nevus) with neurocutaneous melanosis: A distinct syndromic entity

3. BMS1 Is Mutated in Aplasia Cutis Congenita

4. Syndrome de Jadassohn‐Schimmelpenning‐Feuerstein‐Mims (Nevus‐sebaceus‐linearis‐Syndrome);Török E;Aktuelle Derm,1988

5. Sebaceous Nevus Syndrome, Central Nervous System Malformations, Aplasia Cutis Congenita, Limbal Dermoid, and Pigmented Nevus Syndrome

Cited by 1 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. Mosaic RASopathies concept: different skin lesions, same systemic manifestations?;Journal of Medical Genetics;2024-01-30

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