Work

The First Case of Genetically Diagnosed Cantu´ Syndrome in China with Mutation in ABCC9

Year: 2019

Type: article

Source: 58th Annual ESPE Meeting (ESPE 2019)

Authors: Tian Shen, Xingxing Zhang, Qiang Cai, Hạixia Chen, Xi Chen, Xinrui Tan

Language: English

Topic: Genetic and rare skin diseases.

Subfield: Genetics

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

OpenAlex ID: W2985153715

FWCI:

Cites:

Cited by:

Related to: 10