Author Correction: Novel mutations in PIEZO1 cause an autosomal recessive generalized lymphatic dysplasia with non-immune hydrops fetalis

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Location: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 2041-1723

Extent: Online-Ressource

Language: Englisch

Notes: online resource.

Bibliographic citation: Author Correction: Novel mutations in PIEZO1 cause an autosomal recessive generalized lymphatic dysplasia with non-immune hydrops fetalis ; volume:10 ; number:1 ; day:26 ; month:4 ; year:2019 ; pages:1 ; date:12.2019
Nature Communications ; 10, Heft 1 (26.4.2019), 1, 12.2019

Classification: Naturwissenschaften

Creator: Fotiou, Elisavet
Martin-Almedina, Silvia
Simpson, Michael A.
Lin, Shin
Gordon, Kristiana
Brice, Glen
Atton, Giles
Jeffery, Iona
Rees, David C.
Mignot, Cyril
Vogt, Julie
Homfray, Tessa
Snyder, Michael P.
Rockson, Stanley G.
Jeffery, Steve
Mortimer, Peter S.
Mansour, Sahar
Ostergaard, Pia

Contributor: SpringerLink (Online service)

DOI: 10.1038/s41467-019-09905-4

URN: urn:nbn:de:101:1-2019051323333251549869

Rights: Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 14.08.2025, 10:45 AM CEST

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Associated

Fotiou, Elisavet
Martin-Almedina, Silvia
Simpson, Michael A.
Lin, Shin
Gordon, Kristiana
Brice, Glen
Atton, Giles
Jeffery, Iona
Rees, David C.
Mignot, Cyril
Vogt, Julie
Homfray, Tessa
Snyder, Michael P.
Rockson, Stanley G.
Jeffery, Steve
Mortimer, Peter S.
Mansour, Sahar
Ostergaard, Pia
SpringerLink (Online service)

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Author Correction: Novel mutations in PIEZO1 cause an autosomal recessive generalized lymphatic dysplasia with non-immune hydrops fetalis

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Other Objects (12)

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Autosomal recessive myotonia congenita in sheep

Genetics of autosomal recessive intellectual disability

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Prenatal diagnosis of autosomal recessive osteopetrosis: a case report

Early clinical management of autosomal recessive polycystic kidney disease

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Genetics of autosomal recessive intellectual disability

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Nephrocalcinosis (enamel renal syndrome) caused by autosomal recessive FAM20A mutationsNephrocalcinosis (Enamel Renal Syndrome) Caused by Autosomal RecessiveFAM20AMutations

Prenatal diagnosis of autosomal recessive osteopetrosis: a case report

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Nephrocalcinosis (enamel renal syndrome) caused by autosomal recessive FAM20A mutationsNephrocalcinosis (Enamel Renal Syndrome) Caused by Autosomal RecessiveFAM20AMutations

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