Possible biallelic inheritance in <i>TIE1</i> in a family with congenital lymphedema, intestinal lymphangiectasia and cutis aplasia-Reference-Cited by-同舟云学术

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Possible biallelic inheritance in TIE1 in a family with congenital lymphedema, intestinal lymphangiectasia and cutis aplasia

Published:2023-04-24 Issue:2 Volume:104 Page:275-276
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:Clinical Genetics

Author:

Abu Shtaya Aasem¹,Sukenik‐Halevy Rivka²³^ORCID,Bazak Lily¹,Lidzbarsky Gabriel Arie¹,Gonzaga‐Jauregui Claudia⁴^ORCID,Lagovsky Irina⁵,Goldberg Yael¹²,Basel‐Salmon Lina¹²⁵⁶

Affiliation:

1. Recanati Genetic Institute Rabin Medical Center – Beilinson Hospital Petach Tikva Israel

2. Sackler Faculty of Medicine Tel Aviv University Tel Aviv Israel

3. Genetics Institute Meir Medical Center Kfar Saba Israel

4. Regeneron Genetics Center Regeneron Pharmaceuticals Inc. Tarrytown New York USA

5. Felsenstein Medical Research Center Rabin Medical Center – Beilinson Hospital Petach Tikva Israel

6. Pediatric Genetics Clinic Schneider Children's Medical Center of Israel Petach Tikva Israel

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/cge.14344

Reference5 articles.

1. Primary intestinal lymphangiectasia in children: A review

2. Genetics of lymphatic anomalies

3. Tie1 controls angiopoietin function in vascular remodeling and inflammation

4. Characterization of ANGPT2 mutations associated with primary lymphedema

5. TIE1 as a Candidate Gene for Lymphatic Malformations with or without Lymphedema

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