# Mutations in the activin receptor–like kinase 1 gene in hereditary haemorrhagic telangiectasia type 2

**Type:** Papers  
**Canonical URL:** https://scholariq.org/papers/mutations-in-the-activin-receptor-like-kinase-1-gene-in-hereditary-haemorrhagic/

## Facts

| Field | Value |
| --- | --- |
| Author Names | David W. Johnson,Jonathan Berg,Melanie A. Baldwin,Carol J. Gallione,Ivonne Marondel,Sang-Heon Yoon,Timothy T. Stenzel,Marcy C. Speer,M. A. Pericak‐Vance,Austin G. Diamond,Alan E. Guttmacher,Charles E. Jackson,Liliana Attisano,Raju Kucherlapati,Mary Porteous,Douglas A. Marchuk |
| Citations | 1,130 |
| DOI | 10.1038/ng0696-189 |
| Fields | Medicine |
| Open Access | false |
| OA Status | closed |
| OpenAlex ID | https://openalex.org/W2075998623 |
| PMID | 8640225 |
| Type | article |
| Year | 1996 |

## Paper authors

- [David W. Johnson](https://scholariq.org/researchers/david-w-johnson/)

## Paper primary topic

- [Vascular Anomalies and Treatments](https://scholariq.org/topics/vascular-anomalies-and-treatments/)

## Paper topics

- [Vascular Anomalies and Treatments](https://scholariq.org/topics/vascular-anomalies-and-treatments/)
- [Tracheal and airway disorders](https://scholariq.org/topics/tracheal-and-airway-disorders/)
- [Pulmonary Hypertension Research and Treatments](https://scholariq.org/topics/pulmonary-hypertension-research-and-treatments/)

---
Source: ScholarIQ — public research metadata, principally OpenAlex. See https://scholariq.org/sources/ for provenance and https://scholariq.org/methodology/ for what these figures mean.