Work

Expanding the MYBPC1 phenotypic spectrum: a novel homozygous mutation causes arthrogryposis multiplex congenita

Year: 2015

Type: article

Source: Clinical Genetics

DOI: 10.1111/cge.12707

Authors: N. Ekhilevitch, A. Kurolap, D. Oz‐Levi, A. Mory, T. Hershkovitz, G. Ast, H. Mandel, H.N. Baris

Institutions: Rambam Health Care Campus, Tel Aviv University, Technion – Israel Institute of Technology

Language: English

Topic: Congenital limb and hand anomalies

Subfield: Developmental Biology

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

OpenAlex ID: W2193025529

FWCI: 1.442

Cites: 26

Cited by: 21

Related to: 10