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Novel changes in the SLC16A2 gene identified by X-exome sequencing in two Finnish families with Allan-Herndon Dudley syndrome

Year: 2013

Type: article

Source: European Journal of Human Genetics

Authors: AK Philips, Maria Arvio, H Kääriäinen, Hilde Van Esch, Siegfried Haas, Kalscheuer, Guy Froyen, Irma Järvelä

Language: English

Topic: Metabolism and Genetic Disorders

Subfield: Clinical Biochemistry

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

OpenAlex ID: W2525365498

FWCI:

Cites:

Cited by: 1

Related to: 10