Mutations in PROP1 cause familial combined pituitary hormone deficiency

Wu, Wei, Cogan, Joy D., Pfäffle, Roland W., Dasen, Jeremy S., Frisch, Herwig, O'Connell, Shawn M., Flynn, Sarah E., Brown, Milton R., Mullis, Primus E., Parks, John S., Phillips III, John A., Rosenfeld, Michael G.·1998·Nature Genetics

DOI 10.1038/ng0298-147

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Authors: Wu, W., Cogan, J. D., Pfäffle, R. W., Dasen, J. S., Frisch, H., O'Connell, S. M., Flynn, S. E., Brown, M. R., Mullis, P. E., Parks, J. S., Phillips III, J. A., & Rosenfeld, M. G.
Venue: Nature Genetics
Publisher: Springer Science and Business Media LLC
Published: 1998-02
Volume: 18
Issue: 2
Pages: 147-149
ISSN: 1061-4036 (ISSN-L)
1546-1718
DOI: 10.1038/ng0298-147
OpenAlex: W2111626274
Cited by: 568
References: 0
FWCI: 27.92
Type: journal article
Language: en
Open access: closed

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