Work

X-linked hypophosphatemia (XLH): Mutations compromising PHEX structure reflect a severe phenotype

Year: 1999

Type: article

Source: The American Journal of Human Genetics

Authors: Michael P. Whyte, Paul T. Christie, M N Podgornik, Peter H. Dixon, Mitch Eddy, C Wooding, Dorothy Trump, Marvin Grieff, Steven Mumm, D Shlessinger, Rajesh V. Thakker

Language: English

Topic: Parathyroid Disorders and Treatments

Subfield: Nephrology

Field: Medicine

Domain: Health Sciences

SDG: Good health and well-being

Open Access status: closed

OpenAlex ID: W2785009064

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