Work

A novel ROMK mutation in a child presenting with Bartter Syndrome Type 2

Year: 2007

Type: article

Source: Pediatric Nephrology

Authors: Mobin Malik, Louise S. Conwell, Daniel G. Bichet, Etienne Sochett, Donald Hebert

Language: English

Topic: Ion Transport and Channel Regulation

Subfield: Molecular Biology

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

Funders: U.S. Department of Health and Human Services, National Institute on Aging, National Institute of Mental Health, National Institute of General Medical Sciences, National Institute of Neurological Disorders and Stroke, National Institute of Arthritis and Musculoskeletal and Skin Diseases

Awards: G2651823201, G3577467031, Alzheimer's Gut Microbiome Project, G493522462, Graduate Training in Cellular and Molecular Pharmacology, Characterizing the gut microbiome in schizophrenia: Relationship to age, cognition, & disease-related factors, G6129969428, Role of Human-Specific Cathepsin V Protease in the Production of Opioid and Related Peptide Neurotransmitters, G7924948224, G84312951, Rheumatic Diseases Research Training Grant

OpenAlex ID: W34741130

FWCI:

Cites: 36

Cited by:

Related to: 10