Severe early-onset overgrowth in a case of pseudohypoparathyroidism type 1b, caused by STX16 deletion

Autor:	Niels Vos, Leonie A. Menke, Christiaan F. Mooij, Erica L. T. van den Akker, Mariëlle Alders, Mieke M. van Haelst
Přispěvatelé:	Pediatrics, Human genetics, Amsterdam Neuroscience - Complex Trait Genetics, Amsterdam Reproduction & Development (AR&D), Graduate School, General Paediatrics, ANS - Cellular & Molecular Mechanisms, ANS - Complex Trait Genetics, ARD - Amsterdam Reproduction and Development, Paediatric Endocrinology, Human Genetics, ACS - Pulmonary hypertension & thrombosis
Jazyk:	angličtina
Rok vydání:	2023
Předmět:	Genetics Genetics (clinical)
Zdroj:	American Journal of Medical Genetics, Part A, 191(5), 1476-1478. Wiley-Liss Inc. American journal of medical genetics. Part A, 191(5), 1476-1478. Wiley-Liss Inc. Vos, N, Menke, L A, Mooij, C F, van den Akker, E L T, Alders, M & van Haelst, M M 2023, ' Severe early-onset overgrowth in a case of pseudohypoparathyroidism type 1b, caused by STX16 deletion ', American Journal of Medical Genetics, Part A, vol. 191, no. 5, pp. 1476-1478 . https://doi.org/10.1002/ajmg.a.63154
ISSN:	1552-4825
DOI:	10.1002/ajmg.a.63154
Databáze:	OpenAIRE
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