guest ::
Challenges in establishing genotype-phenotype correlations in ARPKD: case report on a toddler with two severe PKHD1 mutations
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In
Pediatric nephrology 32(7), Seiten/Artikel-Nr.:1269-1273
2017
Online
DOI: 10.1007/s00467-017-3648-x
Einrichtungen
Dokumenttyp
Journal Article
Format
online
Sprache
English
Anmerkung
Peer reviewed article
Externe Identnummern
SCOPUS: SCOPUS:2-s2.0-85016455667
WOS Core Collection: WOS:000401926600021
PubMed: pmid:28364132
OpenAlex: W2600866046
Interne Identnummern
RWTH-CONV-221586
Datensatz-ID: 716285
Beteiligte Länder
Germany
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