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Pseudohypoaldosteronism in eight families: Different forms of inheritance are evidence for various genetic defects

par Kuhnle, Ursula;Knorr, Dietrich;Nielsen, Meta Damkjær;Tietze, Hans Ulrich;Schroeter, C.H. C.H.;Schlamp, Dieter;Bosson, Danièle ;Armanini, Decio
Référence The Journal of clinical endocrinology and metabolism, 70, 3, page (638-641)
Publication Publié, 1990

Article révisé par les pairs

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Titre:	Pseudohypoaldosteronism in eight families: Different forms of inheritance are evidence for various genetic defects
Auteur:	Kuhnle, Ursula; Knorr, Dietrich; Nielsen, Meta Damkjær; Tietze, Hans Ulrich; Schroeter, C.H. C.H.; Schlamp, Dieter; Bosson, Danièle; Armanini, Decio
Informations sur la publication:	The Journal of clinical endocrinology and metabolism, 70, 3, page (638-641)
Statut de publication:	Publié, 1990
Sujet CREF:	Biochimie
	Médecine clinique [chimie clinique]
	Endocrinologie
	Métabolisme
	Diabétologie
Note générale:	SCOPUS: ar.j
Langue:	Anglais
Identificateurs:	urn:issn:0021-972X
	info:scp/0025305359
	info:pmid/2137831