Missense mutations in the NDP gene in patients with a less severe course of norrie disease

Alfons Meindl; Bright Lorenz; Helene Achatz; Heide Hellebrand; Peter Schmitz-valckenberg; Thomas Meitinger

doi:10.1093/hmg/4.3.489

Missense mutations in the NDP gene in patients with a less severe course of norrie disease

Alfons Meindl
, Bright Lorenz
, Helene Achatz
, Heide Hellebrand
, Peter Schmitz-valckenberg
, Thomas Meitinger

Ludwig-Maximilians-Universität München
University of Regensburg
Evangel

Research output: Contribution to journal › Comment/debate

55 Scopus citations

Original language	English
Pages (from-to)	489-490
Number of pages	2
Journal	Human Molecular Genetics
Volume	4
Issue number	3
DOIs	https://doi.org/10.1093/hmg/4.3.489
State	Published - Mar 1995
Externally published	Yes

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title = "Missense mutations in the NDP gene in patients with a less severe course of norrie disease",

author = "Alfons Meindl and Bright Lorenz and Helene Achatz and Heide Hellebrand and Peter Schmitz-valckenberg and Thomas Meitinger",

note = "Funding Information: We thank Jan Murken for critical comments. This work was supported by the Deutsche Forschungsgemeinschaft (A.M. and T.M).",

year = "1995",

month = mar,

doi = "10.1093/hmg/4.3.489",

language = "English",

volume = "4",

pages = "489--490",

journal = "Human Molecular Genetics",

issn = "0964-6906",

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T1 - Missense mutations in the NDP gene in patients with a less severe course of norrie disease

AU - Meindl, Alfons

AU - Lorenz, Bright

AU - Achatz, Helene

AU - Hellebrand, Heide

AU - Schmitz-valckenberg, Peter

AU - Meitinger, Thomas

N1 - Funding Information: We thank Jan Murken for critical comments. This work was supported by the Deutsche Forschungsgemeinschaft (A.M. and T.M).

PY - 1995/3

Y1 - 1995/3

UR - https://www.scopus.com/pages/publications/0028901919

U2 - 10.1093/hmg/4.3.489

DO - 10.1093/hmg/4.3.489

M3 - Comment/debate

C2 - 7795608

AN - SCOPUS:0028901919

SN - 0964-6906

VL - 4

SP - 489

EP - 490

JO - Human Molecular Genetics

JF - Human Molecular Genetics

IS - 3

ER -

Missense mutations in the NDP gene in patients with a less severe course of norrie disease

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