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Human ABL1 deficiency syndrome (HADS) is a recognizable syndrome distinct from ABL1-related congenital heart defects and skeletal malformations syndrome

Crossref DOI link: https://doi.org/10.1007/s00439-024-02677-y

Published Online: 2024-05-14

Published Print: 2024-06

Update policy: https://doi.org/10.1007/springer_crossmark_policy

Authors

AlAbdi, Lama

Neuhann, Teresa

Prott, Eva-Christina

Schön, Ulrike

Abdulwahab, Firdous

Faqeih, Eissa

Alkuraya, Fowzan S.
Funding

Funding for this research was provided by:

King Fahad Medical City (IRF 019-052)
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Text and Data Mining valid from 2024-05-14

Version of Record valid from 2024-05-14
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Article History

Received: 15 February 2024

Accepted: 4 May 2024

First Online: 14 May 2024

Declarations

:

: Authors declare no conflicts of interest.

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