Expanding the Phenotypic Spectrum of Mecom-Associated Syndrome: Rare Variants Are Associated with Syndromic Pulmonary Arterial Hypertension

AuthID
 P-01B-3HD
23
Author(s)
Welch, CL
·
McEntagart, M
·
Moledina, S
·
Morgan, C
·
Swietlik, E
·
Hou, C
·
Qiao, L
·
Callejo, E
·
Craib, S
·
Smedley, D
·
[+3]·
Dagan, T
·
Eason, J
·
Flinter, F
·
Joshi, A
·
Mortreux, J
·
Ruiz, FE
·
Shears, D
·
Varghese, NP
·
Chung, WK
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Document Type
Article in Press
Year published
2026
Published
in JOURNAL OF MEDICAL GENETICS, ISSN: 0022-2593
Pages: jmg-2025-111027 (10)
Indexing
Wos®
Scopus®
Crossref®
Pubmed®
Google Scholar®
Publication Identifiers
Pubmed: 41617498
Scopus: 2-s2.0-105029141655
Wos: WOS:001677041100001
Source Identifiers
ISSN: 0022-2593
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All authors
Name Order Name   Name Order Name   Name Order Name
1 Welch, CL;   2 McEntagart, M;   3 Moledina, S;
4 Morgan, C;   5 Swietlik, E;   6 Hou, C;
7 Qiao, L;   8 Callejo, E;   9 Craib, S;
10 Smedley, D;   11 Bijlsma, EK;   12 Bouvagnet, P;
13 Cortes-Santiago, N;   14 Dagan, T;   15 Eason, J;
16 Flinter, F;   17 Joshi, A;   18 Mortreux, J;
19 Ruiz, FE;   20 Shears, D;   21 Soares, CA ;
22 Varghese, NP;   23 Chung, WK;  

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